Original source

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

Alleles
T/C | Ancestral: T | Ambiguity code: Y | MAF: < 0.01 (C)
Location

Chromosome 1:167219393 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.167219393T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad, Illumina_1M-duo

Variation displays