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

This variant has 2 HGVS names - click the plus to show

About this variant

This variant overlaps 1 transcript and has 8 sample genotypes.

Variant displays