Original source

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

Alleles
C/T|Ancestral: C|Ambiguity code: Y
Location

Chromosome 7:44149763 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM970636

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

Synonyms

LSDB GCK_676G_A_060311

HGVS names

This variant has 11 HGVS names - Show

About this variant

This variant overlaps 9 transcripts, is associated with 1 phenotype and is mentioned in 6 citations.

Variant displays