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: rs104894140
rs104894140
2 0.925 0.200 10 102830979 missense variant A/C snv 0.010 1.000 1 2000 2000
dbSNP: rs104894148
rs104894148
2 0.925 0.200 10 102835343 missense variant T/A snv 0.010 1.000 1 2002 2002
dbSNP: rs104894150
rs104894150
1 1.000 10 102834850 missense variant A/C;T snv 4.0E-06; 1.2E-05 0.010 1.000 1 2005 2005
dbSNP: rs104894152
rs104894152
1 1.000 10 102837281 stop gained G/T snv 0.010 1.000 1 2015 2015
dbSNP: rs760695410
rs760695410
6 0.807 0.240 10 102832532 missense variant T/A snv 1.2E-05; 4.0E-06 0.010 1.000 1 2001 2001