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Select item 714236071.

rs71423607 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:233651679 (GRCh38)
2:234560325 (GRCh37)
Canonical SPDI:: NC_000002.12:233651678:C:G
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.055003/1039 (ALFA)
G=0./0 (KOREAN)
G=0.002183/4 (Korea1K)
G=0.02639/132 (1000Genomes)
G=0.039509/177 (Estonian)
G=0.046799/6561 (GnomAD)
G=0.048358/12800 (TOPMED)
G=0.067462/260 (ALSPAC)
G=0.074434/276 (TWINSUK)
G=0.075/3 (GENOME_DK)
G=0.078156/78 (GoNL)
G=0.083333/18 (Qatari)
G=0.09/54 (NorthernSweden)
C=0.466667/14 (SGDP_PRJ)
HGVS:: NC_000002.12:g.233651679C>G, NC_000002.11:g.234560325C>G, NG_002601.2:g.66936C>G

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