Original source

Variants (including SNPs and indels) imported from dbSNP (release 142) | View in dbSNP

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.03 (C)
Location

Chromosome 16:31178652 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

16:g.31178652A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

About this variant

This variant overlaps 9 transcripts and has 2505 individual genotypes.

Variation displays