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: rs1332619445
rs1332619445
AR
1 1.000 0.160 X 67717542 missense variant G/C snv 0.010 1.000 1 2007 2007
dbSNP: rs137852562
rs137852562
AR
2 0.925 0.160 X 67721837 missense variant C/T snv 0.010 1.000 1 2003 2003
dbSNP: rs137852591
rs137852591
AR
4 0.851 0.200 X 67721909 missense variant C/G snv 1.4E-03 1.4E-03 0.010 1.000 1 2017 2017
dbSNP: rs1410383824
rs1410383824
AR
2 0.925 0.160 X 67546470 stop gained G/A;T snv 0.010 < 0.001 1 2010 2010
dbSNP: rs556339046
rs556339046
MSH6 ; FBXO11
1 1.000 0.160 2 47800218 missense variant T/G snv 3.6E-05 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs886041132
rs886041132
AR
2 0.925 0.160 X 67722943 missense variant C/T snv 0.010 1.000 1 2004 2004
dbSNP: rs9332971
rs9332971
AR
4 0.851 0.200 X 67722944 missense variant G/A;T snv 0.010 1.000 1 2004 2004