Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.01 (A)
Location

Chromosome 1:169513937 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.169513937T>A

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 3 transcripts and has 2504 individual genotypes.

Variation displays