Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | 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
Intron variant
Evidence status


Archive dbSNP rs586624

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 10 transcripts and has 2807 sample genotypes.

Variant displays