Original source

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

Alleles
T/C | Ancestral: C | Ambiguity code: Y | MAF: 0.37 (C)
Location

Chromosome 3:171027026 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR025511

Most severe consequence
Evidence status

HGVS name

3:g.171027026T>C

Genotyping chips

This variation has assays on: Illumina_Cardio-Metabo_Chip, Illumina_1M-duo

Variation displays