rs1518110 - SNP

Select item 15181101.

rs1518110 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 1:206771516 (GRCh38)
1:206944861 (GRCh37)
Canonical SPDI:: NC_000001.11:206771515:A:C,NC_000001.11:206771515:A:G,NC_000001.11:206771515:A:T
Gene:: IL10 (Varview), IL19 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.264874/5111 (ALFA)
A=0.196872/730 (TWINSUK)
A=0.203166/783 (ALSPAC)
A=0.209419/209 (GoNL)
A=0.213333/128 (NorthernSweden)
A=0.220956/989 (Estonian)
A=0.225/9 (GENOME_DK)
A=0.277778/60 (Qatari)
A=0.279018/125 (SGDP_PRJ)
C=0.283019/60 (Vietnamese)
A=0.288462/15 (Siberian)
A=0.291011/40670 (GnomAD)
C=0.301365/883 (KOREAN)
C=0.307314/563 (Korea1K)
A=0.313589/83004 (TOPMED)
C=0.359924/6032 (TOMMO)
A=0.420518/2106 (1000Genomes)
HGVS:: NC_000001.11:g.206771516A>C, NC_000001.11:g.206771516A>G, NC_000001.11:g.206771516A>T, NC_000001.10:g.206944861A>C, NC_000001.10:g.206944861A>G, NC_000001.10:g.206944861A>T, NG_012088.1:g.5979T>G, NG_012088.1:g.5979T>C, NG_012088.1:g.5979T>A

Select item 3865352972.

rs386535297 has merged into rs1518110 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 1:206771516 (GRCh38)
1:206944861 (GRCh37)
Canonical SPDI:: NC_000001.11:206771515:A:C,NC_000001.11:206771515:A:G,NC_000001.11:206771515:A:T
Gene:: IL10 (Varview), IL19 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.264874/5111 (ALFA)
A=0.196872/730 (TWINSUK)
A=0.203166/783 (ALSPAC)
A=0.209419/209 (GoNL)
A=0.213333/128 (NorthernSweden)
A=0.220956/989 (Estonian)
A=0.225/9 (GENOME_DK)
A=0.277778/60 (Qatari)
A=0.279018/125 (SGDP_PRJ)
C=0.283019/60 (Vietnamese)
A=0.288462/15 (Siberian)
A=0.291011/40670 (GnomAD)
C=0.301365/883 (KOREAN)
C=0.307314/563 (Korea1K)
A=0.313589/83004 (TOPMED)
C=0.359924/6032 (TOMMO)
A=0.420518/2106 (1000Genomes)
HGVS:: NC_000001.11:g.206771516A>C, NC_000001.11:g.206771516A>G, NC_000001.11:g.206771516A>T, NC_000001.10:g.206944861A>C, NC_000001.10:g.206944861A>G, NC_000001.10:g.206944861A>T, NG_012088.1:g.5979T>G, NG_012088.1:g.5979T>C, NG_012088.1:g.5979T>A

Select item 37486743.

rs3748674 has merged into rs1518110 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 1:206771516 (GRCh38)
1:206944861 (GRCh37)
Canonical SPDI:: NC_000001.11:206771515:A:C,NC_000001.11:206771515:A:G,NC_000001.11:206771515:A:T
Gene:: IL10 (Varview), IL19 (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.264874/5111 (ALFA)
A=0.196872/730 (TWINSUK)
A=0.203166/783 (ALSPAC)
A=0.209419/209 (GoNL)
A=0.213333/128 (NorthernSweden)
A=0.220956/989 (Estonian)
A=0.225/9 (GENOME_DK)
A=0.277778/60 (Qatari)
A=0.279018/125 (SGDP_PRJ)
C=0.283019/60 (Vietnamese)
A=0.288462/15 (Siberian)
A=0.291011/40670 (GnomAD)
C=0.301365/883 (KOREAN)
C=0.307314/563 (Korea1K)
A=0.313589/83004 (TOPMED)
C=0.359924/6032 (TOMMO)
A=0.420518/2106 (1000Genomes)
HGVS:: NC_000001.11:g.206771516A>C, NC_000001.11:g.206771516A>G, NC_000001.11:g.206771516A>T, NC_000001.10:g.206944861A>C, NC_000001.10:g.206944861A>G, NC_000001.10:g.206944861A>T, NG_012088.1:g.5979T>G, NG_012088.1:g.5979T>C, NG_012088.1:g.5979T>A

dbSNP