Original source

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

Alleles
G/A | Ancestral: G | Ambiguity code: R | MAF: 0.20 (A)
Location

Chromosome 9:95282923 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs491539, rs56547230

This variation has 8 HGVS names - click the plus to show

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Affy GenomeWideSNP_6.0

Variation displays