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: 0.01 (A)
Location

Chromosome 3:170995925 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

3:g.170995925G>A

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip

Variation displays