Original source

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

Alleles
T/A | Ancestral: T | Ambiguity code: W | MAF: 0.49 (A)
Location

Chromosome 10:111075832 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.111075832T>A

This variation has assays on 7 chips - click the plus to show

Variation displays