Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.29 (A)
Location

Chromosome 10:122461028 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR065642

Most severe consequence
Evidence status

Clinical significance

HGVS name

10:g.122461028G>A

Genotyping chips

This variation has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, has 2505 individual genotypes, is associated with 2 phenotypes and is mentioned in 149 citations.

Variation displays