Original source

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

Alleles
G/C | Ancestral: C | Ambiguity code: S | MAF: 0.01 (C)
Location

Chromosome 11:34437324 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.34437324G>C

About this variant

This variant overlaps 1 transcript and has 2504 individual genotypes.

Variation displays