Original source

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

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

Chromosome 11:68978580 (forward strand) | View in location tab

Most severe consequence
Evidence status

HGVS name

11:g.68978580G>A

This variation has assays on 6 chips - click the plus to show

Variation displays