Original source

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

Alleles
G/A/C | Ancestral: G | Ambiguity code: V | MAF: < 0.01 (C)
Location

Chromosome 4:6301739 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM982041

Most severe consequence
 
Stop gained
Evidence status

Clinical significance

Synonyms

LSDB 2010_April_001_086_WFS1_606201_0005, 13626

This variant has 12 HGVS names - click the plus to show

About this variant

This variant overlaps 10 transcripts, has 2504 sample genotypes and is associated with 2 phenotypes.

Variant displays