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
Evidence status

Clinical significance

This variation has 4 synonyms - click the plus to show

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

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

About this variant

This variant overlaps 7 transcripts, has 2507 individual genotypes, is associated with 4 phenotypes and is mentioned in 4 citations.

Variation displays