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: 0.50 (C)
Location

Chromosome 7:22823103 (forward strand) | View in location tab

Most severe consequence
Evidence status

Synonyms

Archive dbSNP rs59513014

HGVS name

7:g.22823103C>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays