Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.04 (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 1096 individual genotypes.

Variation displays