Original source

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

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.03 (T)
Location

Chromosome 9:122202160 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

9:g.122202160C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 12 transcripts and has 2504 individual genotypes.

Variation displays