Original source

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

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.27 (A)

Chromosome 9:99146633 (forward strand) | View in location tab


with HGMD-PUBLIC CS045221

Most severe consequence
Intron variant
Evidence status


Archive dbSNP rs58752737, rs57667361

HGVS names

This variant has 6 HGVS names - Show

Genotyping chips

This variant has assays on 5 chips - Show

About this variant

This variant overlaps 6 transcripts, has 4398 sample genotypes and is mentioned in 7 citations.

Variant displays