Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | [View in dbSNP]

G/A | Ancestral: A | Ambiguity code: R | MAF: 0.29 (A)

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


with HGMD-PUBLIC CS045221

Most severe consequence
Evidence status


Archive dbSNP rs58752737, rs57667361

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

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

About this variant

This variant overlaps 6 transcripts, has 2993 individual genotypes and is mentioned in 6 citations.

Variation displays