Source: ALL
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: rs28934604
rs28934604
CYP27B1
1 1.000 0.200 12 57766073 missense variant C/T snv 0.800 1.000 9 1998 2015
dbSNP: rs118204009
rs118204009
CYP27B1
2 0.925 0.280 12 57764147 missense variant C/T snv 1.0E-04 4.2E-05 0.800 1.000 5 1998 2012
dbSNP: rs28934605
rs28934605
CYP27B1
1 1.000 0.200 12 57766019 missense variant C/T snv 0.800 1.000 5 1998 2002
dbSNP: rs28934606
rs28934606
CYP27B1
1 1.000 0.200 12 57764510 missense variant C/G;T snv 1.2E-05 0.800 1.000 5 1998 2002
dbSNP: rs28934607
rs28934607
CYP27B1
1 1.000 0.200 12 57764169 missense variant G/A snv 0.800 1.000 5 1998 2002
dbSNP: rs118204007
rs118204007
CYP27B1
1 1.000 0.200 12 57764755 missense variant G/C snv 0.800 0
dbSNP: rs118204008
rs118204008
CYP27B1
1 1.000 0.200 12 57763798 missense variant G/A snv 3.6E-05 3.5E-05 0.800 0
dbSNP: rs118204010
rs118204010
CYP27B1
1 1.000 0.200 12 57764148 missense variant G/A;C snv 1.6E-05 0.800 0
dbSNP: rs118204011
rs118204011
CYP27B1
1 1.000 0.200 12 57764487 missense variant G/A snv 0.800 0
dbSNP: rs118204012
rs118204012
CYP27B1
1 1.000 0.200 12 57765320 missense variant T/C snv 0.800 0
dbSNP: rs1057520815
rs1057520815
CYP27B1
1 1.000 0.200 12 57766088 missense variant C/T snv 0.710 1.000 1 2010 2010
dbSNP: rs568165874
rs568165874
CYP27B1
1 1.000 0.200 12 57763738 missense variant C/G;T snv 9.9E-05 0.700 1.000 5 1998 2002
dbSNP: rs1161799032
rs1161799032
CYP27B1
1 1.000 0.200 12 57763179 missense variant G/C snv 1.6E-05 0.700 0
dbSNP: rs387906258
rs387906258
CYP27B1
1 1.000 0.200 12 57765170 frameshift variant C/- delins 0.700 0
dbSNP: rs387906259
rs387906259
CYP27B1
1 1.000 0.200 12 57765108 frameshift variant G/- delins 0.700 0
dbSNP: rs387906260
rs387906260
CYP27B1
1 1.000 0.200 12 57766131 frameshift variant C/- del 3.5E-05 3.5E-05 0.700 0
dbSNP: rs555068245
rs555068245
CYP27B1
1 1.000 0.200 12 57763649 missense variant G/A;C snv 4.8E-05 0.700 0
dbSNP: rs761780097
rs761780097
CYP27B1
1 1.000 0.200 12 57765296 splice donor variant C/G;T snv 8.2E-06 0.700 0
dbSNP: rs767480544
rs767480544
CYP27B1
1 1.000 0.200 12 57763667 missense variant G/A snv 1.6E-05 1.4E-05 0.700 0
dbSNP: rs868704228
rs868704228
CYP27B1
1 1.000 0.200 12 57766847 missense variant C/A snv 0.700 0
dbSNP: rs749037995
rs749037995
PTH
1 1.000 0.200 11 13492551 frameshift variant G/- delins 0.010 1.000 1 2010 2010