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Select item 134024561.

rs13402456 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 2:233656746 (GRCh38)
2:234565392 (GRCh37)
Canonical SPDI:: NC_000002.12:233656745:A:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.050079/946 (ALFA)
T=0.024516/123 (1000Genomes)
T=0.027778/6 (Qatari)
T=0.04/24 (NorthernSweden)
T=0.042374/11216 (TOPMED)
T=0.042873/5996 (GnomAD)
T=0.044866/201 (Estonian)
T=0.05/2 (GENOME_DK)
T=0.062028/230 (TWINSUK)
T=0.062532/241 (ALSPAC)
T=0.072144/72 (GoNL)
A=0.461538/12 (SGDP_PRJ)
A=0.5/2 (Siberian)
HGVS:: NC_000002.12:g.233656746A>T, NC_000002.11:g.234565392A>T, NG_002601.2:g.72003A>T

dbSNP