Original source

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

Alleles
T/A|Ancestral: T|Ambiguity code: W|MAF: 0.15 (A)
Location

Chromosome 10:6080046 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR075253

Most severe consequence
 
Intergenic variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS name

10:g.6080046T>A

Genotyping chips

This variant has assays on 9 chips - Show

About this variant

This variant has 3881 sample genotypes, is associated with 2 phenotypes and is mentioned in 46 citations.

Variant displays