Original source

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

Alleles
C/A|Ancestral: C|Ambiguity code: M|MAF: 0.03 (A)
Location

Chromosome 10:6072697 (forward strand)|View in location tab

Co-located variant

HGMD-PUBLIC CR075252

Most severe consequence
 
Upstream gene variant
Evidence status

Clinical significance

Synonyms

This variant has 2 synonyms - Show

HGVS name

10:g.6072697C>A

Genotyping chips

This variant has assays on: Illumina_ImmunoChip

About this variant

This variant overlaps 1 transcript, 1 regulatory feature, has 2506 sample genotypes, is associated with 2 phenotypes and is mentioned in 23 citations.

Variant displays