Original source

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

This variant has 6 HGVS names - click the plus to show

This variant has assays on 5 chips - click the plus to show

About this variant

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

Variant displays