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: rs104893807
rs104893807
2 0.923 0.107 3 30674196 missense variant C/G,T snp 0.700 2 2004 2012
dbSNP: rs104893815
rs104893815
4 0.846 0.214 3 30691478 missense variant G/A snp 0.700 2 2005 2006
dbSNP: rs28934568
rs28934568
2 0.923 0.107 3 30672106 missense variant T/C snp 0.700 2 2004 2010
dbSNP: rs104893809
rs104893809
2 0.923 0.107 3 30691504 missense variant C/T snp 0.700 1 2004 2004
dbSNP: rs104893810
rs104893810
2 0.923 0.107 3 30691477 missense variant C/T snp 0.700 1 2005 2005
dbSNP: rs104893811
rs104893811
4 0.846 0.143 3 30674228 missense variant C/T snp 0.700 1 2006 2006
dbSNP: rs104893812
rs104893812
2 0.923 0.107 3 30672189 missense variant T/A snp 0.700 1 2005 2005
dbSNP: rs104893813
rs104893813
2 0.923 0.107 3 30672246 missense variant G/A,C,T snp 8.2E-06; 8.2E-06 0.700 1 2005 2005
dbSNP: rs104893814
rs104893814
2 0.923 0.107 3 30672252 stop gained G/T snp 0.700 1 2005 2005
dbSNP: rs104893816
rs104893816
4 0.846 0.107 3 30674229 missense variant G/A snp 4.0E-06 0.700 1 2006 2006
dbSNP: rs193922664
rs193922664
2 0.923 0.107 3 30691435 missense variant T/C snp 0.700 1 2012 2012
dbSNP: rs761231369
rs761231369
1 1.000 0.107 3 30671923 missense variant A/T snp 8.0E-06 3.2E-05 0.700 1 2009 2009
dbSNP: rs780542125
rs780542125
1 1.000 0.107 3 30671752 missense variant G/A snp 5.2E-05 3.2E-05 0.700 1 2009 2009
dbSNP: rs863223853
rs863223853
1 1.000 0.107 3 30691421 missense variant G/T snp 0.700 1 2011 2011
dbSNP: rs886039551
rs886039551
2 0.923 0.107 3 30674186 missense variant G/A snp 0.700 1 2006 2006