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
Location

Chromosome 18:6941245 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

18:g.6941245T>C

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays