Original source

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

A/C | Ancestral: A | Ambiguity code: M | MAF: 0.36 (C)

Chromosome 1:67281732 (forward strand) | View in location tab

Most severe consequence
Downstream gene variant
Evidence status


Archive dbSNP rs56790568

HGVS name


Genotyping chips

This variant has assays on 6 chips - Show

About this variant

This variant overlaps 1 transcript, has 3687 sample genotypes, is associated with 1 phenotype and is mentioned in 4 citations.

Variant displays