Variant: rs397514702 

    present in Gene: WNT1;WNT10B
    present in Chromosome: 12
    Position on Chromosome: 48981179
    Alleles of this Variant: T/G

rs397514702 in WNT1;WNT10B gene and Osteoporosis PMID 23656646 2013 In 10 family members with dominantly inherited, early-onset osteoporosis, we identified a heterozygous missense mutation in WNT1, c.652T→G (p.Cys218Gly).

PMID 23499309 2013 Mutations in WNT1 cause different forms of bone fragility.