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Select item 288991791.

rs28899179 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 2:233702744 (GRCh38)
2:234611390 (GRCh37)
Canonical SPDI:: NC_000002.12:233702743:C:A,NC_000002.12:233702743:C:G,NC_000002.12:233702743:C:T
Gene:: UGT1A10 (Varview), UGT1A8 (Varview), UGT1A7 (Varview), UGT1A6 (Varview), UGT1A9 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000196/6 (ALFA)
A=0./0 (TWINSUK)
A=0.000259/1 (ALSPAC)
A=0.00463/1 (Qatari)
A=0.007651/38 (1000Genomes)
A=0.008947/1254 (GnomAD)
A=0.012195/4 (HapMap)
C=0.5/2 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233702744C>A, NC_000002.12:g.233702744C>G, NC_000002.12:g.233702744C>T, NC_000002.11:g.234611390C>A, NC_000002.11:g.234611390C>G, NC_000002.11:g.234611390C>T, NG_002601.2:g.118001C>A, NG_002601.2:g.118001C>G, NG_002601.2:g.118001C>T

Supplemental Content

dbSNP