Original source

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

Alleles
G/T|Ancestral: G|Ambiguity code: K
Location

Chromosome 4:88046668 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs17417123, rs3191318

HGVS names

This variant has 4 HGVS names - Show

About this variant

This variant overlaps 3 transcripts and has 2 sample genotypes.

Variant displays