Original source

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

G/A | Ancestral: G | Ambiguity code: R | MAF: 0.14 (A)

Chromosome 19:33495473 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs388725, rs253672, rs835582

This variation has 6 HGVS names - click the plus to show

About this variant

This variant overlaps 7 transcripts and has 1356 individual genotypes.

Variation displays