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: 0.01 (T)

Chromosome 19:11379186 (forward strand) | View in location tab

Most severe consequence
Evidence status


Archive dbSNP rs586624

This variation has 8 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts and has 1387 individual genotypes.

Variation displays