Original source

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

G/A | Ancestral: C | Ambiguity code: R | MAF: 0.04 (A)

Chromosome 5:150120233 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs62618696

This variation has 4 HGVS names - click the plus to show

About this variant

This variant overlaps 5 transcripts and has 1093 individual genotypes.

Variation displays