Original source

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

C/T|Ancestral: C|Ambiguity code: Y|MAF: 0.18 (T)

Chromosome 3:137071697 (forward strand)|View in location tab

Most severe consequence
Intergenic variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant has 2507 sample genotypes and is mentioned in 2 citations.

Variant displays