Original source

Variants (including SNPs and indels) imported from dbSNP (release 143) | View in dbSNP

G/A | Ambiguity code: R

Chromosome 4:77459658 (forward strand) | View in location tab

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs17872108

HGVS names

This variant has 2 HGVS names - Show

About this variant

This variant overlaps 1 transcript and has 8 sample genotypes.

Variant displays