Original source

Variants (including SNPs and indels) imported from dbSNP (release 144)|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 variant

HGMD-PUBLIC CR065642

Most severe consequence
 
Upstream gene variant
Evidence status

Clinical significance

Synonyms

LSDB SCV000028119

HGVS name

10:g.122461028G>A

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 161 citations.

Variant displays