Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.13 (A)
Location

Chromosome 10:62655424 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CM033482

Most severe consequence
 
Missense variant
Evidence status

Clinical significance

This variant has 6 synonyms - click the plus to show

This variant has 10 HGVS names - click the plus to show

This variant has assays on 12 chips - click the plus to show

About this variant

This variant overlaps 7 transcripts, 1 regulatory feature, has 2900 sample genotypes, is associated with 4 phenotypes and is mentioned in 9 citations.

Variant displays