Original source

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

Alleles
T/G | Ancestral: T | Ambiguity code: K
Location

Chromosome 11:46718614 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.46718614T>G

Genotyping chips

This variation has assays on: Illumina_HumanOmni1-Quad

Variation displays