Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 2:233031947 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

2:g.233031947A>C

About this variant

This variant overlaps 1 transcript and has 2766 individual genotypes.

Variation displays