Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: 0.14 (C)
Location

Chromosome 16:88809263 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs117716417, rs8191506

HGVS name

16:g.88809263T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 17 transcripts and has 2594 individual genotypes.

Variation displays