Original source

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

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

Chromosome 3:55279372 (forward strand) | View in location tab

Most severe consequence
 
Intergenic variant
Evidence status

HGVS name

3:g.55279372A>C

This variant has assays on 12 chips - click the plus to show

About this variant

This variant has 2730 sample genotypes, is associated with 1 phenotype and is mentioned in 1 citation.

Variant displays