Original source

Variants (including SNPs and indels) imported from dbSNP (mapped to GRCh38) (release 138) | View in dbSNP

Alleles
C/T | Ancestral: C | Ambiguity code: Y | MAF: 0.17 (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

Variation displays