Original source

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

T/A | Ancestral: T | Ambiguity code: W | MAF: 0.31 (A)

Chromosome 22:29280706 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs5763127

This variation has 16 HGVS names - click the plus to show

About this variant

This variant overlaps 16 transcripts and has 1098 individual genotypes.

Variation displays