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Select item 455226391.

rs45522639 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:233637206 (GRCh38)
2:234545852 (GRCh37)
Canonical SPDI:: NC_000002.12:233637205:A:G
Gene:: UGT1A10 (Varview), UGT1A8 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.007/1 (PharmGKB)
HGVS:: NC_000002.12:g.233637206A>G, NC_000002.11:g.234545852A>G, NG_002601.2:g.52463A>G, NM_019075.2:c.684A>G, NM_019075.4:c.684A>G, NM_019075.3:c.684A>G

dbSNP