Original source

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

Alleles
A/T | Ancestral: A | Ambiguity code: W | MAF: 0.03 (T)
Location

Chromosome 1:102876032 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.102876032A>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni2.5, Illumina_HumanOmni5

About this variant

This variant overlaps 5 transcripts and has 2505 individual genotypes.

Variation displays