Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

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

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

Co-located

with HGMD-PUBLIC CM983476

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 13631, 2010_April_001_088_WFS1_606201_0010

This variant has 8 HGVS names - click the plus to show

About this variant

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

Variant displays