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 4:6291961 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CM983476

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 13631, 2010_April_001_088_WFS1_606201_0010

HGVS names

This variant has 8 HGVS names - Show

About this variant

This variant overlaps 6 transcripts and is associated with 2 phenotypes.

Variant displays