Original source

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

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

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


with HGMD-PUBLIC CR065642

Most severe consequence
Upstream gene variant
Evidence status

Clinical significance

HGVS name


Genotyping chips

This variant has assays on: HumanCoreExome-12, Illumina_ExomeChip

About this variant

This variant overlaps 2 transcripts, has 2505 sample genotypes, is associated with 4 phenotypes and is mentioned in 153 citations.

Variant displays