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: 0.21 (C)
Location

Chromosome 16:23181435 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.23181435T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5, Illumina_1M-duo

Variation displays