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: rs10480299
rs10480299
PRKAG2
2 7 151708732 intron variant T/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs11954639
rs11954639
TTC33
1 5 40674877 intron variant C/T snv 8.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs1553091
rs1553091
LOC107986166
1 3 187999098 intron variant A/G snv 0.28 0.700 1.000 1 2019 2019
dbSNP: rs17663555
rs17663555
LOC105379030
3 1.000 0.080 5 73136209 intron variant C/A;G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2003313
rs2003313 		1 11 111333268 intergenic variant A/T snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs2503107
rs2503107
RSPO3
1 6 127142231 intron variant C/A snv 0.56 0.700 1.000 1 2019 2019
dbSNP: rs4686914
rs4686914
LOC107986166
3 3 187999752 intron variant C/T snv 0.27 0.700 1.000 1 2019 2019
dbSNP: rs795230
rs795230
LOC101928338
1 11 30752978 intergenic variant C/T snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs914615
rs914615
THBS3
1 1 155206101 intron variant G/A snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs998394
rs998394
ADAMTS9-AS2
2 3 64815512 intron variant A/G snv 0.62 0.700 1.000 1 2019 2019