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Select item 455700331.

rs45570033 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:233671357 (GRCh38)
2:234580003 (GRCh37)
Canonical SPDI:: NC_000002.12:233671356:A:C
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A9 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.001942/28 (ALFA)
C=0./0 (ALSPAC)
C=0.00027/1 (TWINSUK)
C=0.001405/7 (1000Genomes)
C=0.00298/418 (GnomAD)
C=0.003245/859 (TOPMED)
C=0.020833/3 (PharmGKB)
A=0.5/3 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233671357A>C, NC_000002.11:g.234580003A>C, NG_002601.2:g.86614A>C

dbSNP