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 3:58428515 (forward strand)|View in location tab

Most severe consequence
 
Missense variant
Evidence status

Synonyms

Archive dbSNP rs11542398

HGVS names

This variant has 13 HGVS names - Show

About this variant

This variant overlaps 20 transcripts and has 2 sample genotypes.

Variant displays