Original source

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

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

Chromosome 3:170744815 (forward strand) | View in location tab

Co-located

with HGMD-PUBLIC CR025511

Most severe consequence
Evidence status

HGVS name

3:g.170744815T>C

Genotyping chips

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

Variation displays