Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.09 (C)

Chromosome 1:247922126 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status

HGVS name


Genotyping chips

This variant has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 1 transcript and has 2845 sample genotypes.

Variant displays