Original source

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

A/T | Ancestral: A | Ambiguity code: W | MAF: 0.03 (A)

Chromosome 19:33496679 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs253673, rs3826902

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

About this variant

This variant overlaps 7 transcripts and has 1392 individual genotypes.

Variation displays