Original source

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

Alleles
A/C | Ancestral: A | Ambiguity code: M | MAF: 0.01 (C)
Location

Chromosome 13:48231375 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

13:g.48231375A>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays