Original source

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

Alleles
A/G | Ancestral: A | Ambiguity code: R | MAF: 0.12 (G)
Location

Chromosome 10:50815696 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

10:g.50815696A>G

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

Variation displays