Original source

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

Alleles
G/A|Ambiguity code: R
Location

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

Most severe consequence
 
Intron variant
Evidence status

Synonyms

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