Original source

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

Alleles
G/A | Ancestral: A | Ambiguity code: R | MAF: 0.15 (A)
Location

Chromosome 4:154570607 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM080365

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 6 synonyms - click the plus to show

This variant has 6 HGVS names - click the plus to show

This variant has assays on 11 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, has 4370 sample genotypes, is associated with 2 phenotypes and is mentioned in 12 citations.

Variant displays