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Select item 356407821.

rs35640782 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:233765768 (GRCh38)
2:234674414 (GRCh37)
Canonical SPDI:: NC_000002.12:233765767:G:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A5 (Varview), UGT1A9 (Varview), UGT1A4 (Varview), UGT1A1 (Varview), UGT1A3 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.011073/285 (ALFA)
T=0.00027/1 (TWINSUK)
T=0.000778/3 (ALSPAC)
T=0.022868/3201 (GnomAD)
T=0.024361/6448 (TOPMED)
T=0.027778/6 (Qatari)
T=0.033573/168 (1000Genomes)
G=0.4/4 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233765768G>T, NC_000002.11:g.234674414G>T, NG_002601.2:g.181025G>T, NG_033238.1:g.10496G>T

Supplemental Content

dbSNP