Original source

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

T/G | Ancestral: T | Ambiguity code: K | MAF: < 0.01 (G)

Chromosome 2:9583725 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 4 transcripts and has 2504 sample genotypes.

Variant displays