Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.03 (G)
Location

Chromosome 9:122202268 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.122202268A>G

About this variant

This variant overlaps 12 transcripts and has 2506 individual genotypes.

Variation displays