Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.05 (G)
Location

Chromosome 10:71730514 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM021540

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 4 synonyms - click the plus to show

This variant has 11 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

This variant overlaps 6 transcripts, 1 regulatory feature, has 2507 sample genotypes, is associated with 5 phenotypes and is mentioned in 4 citations.

Variant displays