Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs199476310
rs199476310
1 15 63057019 missense variant T/C snv 0.700 1.000 2 2010 2011
dbSNP: rs199476311
rs199476311
1 15 63059667 missense variant G/A snv 0.700 1.000 1 2010 2010
dbSNP: rs199476317
rs199476317
4 0.827 0.080 15 63062263 missense variant G/A snv 0.700 1.000 1 2010 2010
dbSNP: rs397516364
rs397516364
1 0.925 0.080 15 63042852 missense variant T/G snv 0.700 1.000 1 2000 2000
dbSNP: rs397516370
rs397516370
1 15 63057085 missense variant A/G snv 0.700 1.000 1 2011 2011
dbSNP: rs397516363
rs397516363
1 15 63044075 missense variant G/A snv 0.700 0
dbSNP: rs397516369
rs397516369
2 1.000 15 63057081 missense variant C/G snv 0.700 0
dbSNP: rs397516371
rs397516371
1 15 63059611 missense variant G/C snv 0.700 0
dbSNP: rs397516373
rs397516373
4 0.925 0.080 15 63059663 missense variant G/A snv 0.700 0
dbSNP: rs727504389
rs727504389
1 15 63059604 missense variant A/T snv 0.700 0
dbSNP: rs876657662
rs876657662
1 15 63060872 stop gained G/A snv 0.700 0