Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

A/C | Ancestral: C | Ambiguity code: M | MAF: 0.28 (A)

Chromosome 12:132629721 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs6560892, rs59140641

This variation has 9 HGVS names - click the plus to show

About this variant

This variant overlaps 13 transcripts and has 1115 individual genotypes.

Variation displays