Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.07 (C)
Location

Chromosome 1:248085428 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

1:g.248085428A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays