Original source

Variants (including SNPs and indels) imported from dbSNP (release 144) | View in dbSNP

G/A | Ancestral: A | Ambiguity code: R

Chromosome 17:47578557 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs2644358

HGVS names

This variant has 12 HGVS names - Show

About this variant

This variant overlaps 13 transcripts and has 1 sample genotype.

Variant displays