Original source

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

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

Chromosome 7:38976022 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs17175586

HGVS name

7:g.38976022C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

About this variant

This variant overlaps 2 transcripts and has 2579 individual genotypes.

Variation displays