Original source

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

Alleles
G/T | Ancestral: G | Ambiguity code: K | MAF: 0.01 (T)
Location

Chromosome 7:2537850 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

7:g.2537850G>T

Genotyping chips

This variation has assays on: Illumina_HumanOmni5

Variation displays