Original source

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

Alleles
A/G | Ancestral: G | Ambiguity code: R | MAF: 0.38 (A)
Location

Chromosome 10:102063378 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.102063378A>G

This variation has assays on 4 chips - click the plus to show

Variation displays