Source: UNIPROT

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs397514702
rs397514702
WNT1 ; WNT10B
1.000 0.080 12 48981179 missense variant T/G snv 4.9E-05 7.0E-06
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.740 1.000 2 2013 2019
dbSNP: rs387907359
rs387907359
WNT1 ; WNT10B
1.000 0.080 12 48981230 missense variant C/T snv
CUI: C0029456
Disease: Osteoporosis
Osteoporosis 		0.700 0