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: rs10003632
rs10003632
IQCM
1 4 149563756 missense variant G/T snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10191770
rs10191770 		1 2 114179758 intergenic variant T/C snv 8.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs10485552
rs10485552
KIF16B
1 20 16451011 intron variant T/C snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs16895119
rs16895119
QKI
1 6 163576234 3 prime UTR variant C/T snv 4.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs17065527
rs17065527
PTPRG
1 3 61864416 intron variant G/A snv 2.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs2015232
rs2015232 		1 11 123876886 intergenic variant G/A snv 4.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs2465625
rs2465625 		1 12 46956964 regulatory region variant G/T snv 0.98 0.700 1.000 1 2012 2012
dbSNP: rs3924703
rs3924703
ADGRL2
1 1 81478514 intron variant A/G snv 3.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs4800181
rs4800181
OSBPL1A
1 18 24208783 intron variant G/A snv 0.94 0.700 1.000 1 2012 2012
dbSNP: rs551312
rs551312
CASP17P
1 11 104916246 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs6803364
rs6803364
LOC105377095
1 3 54002671 intergenic variant T/G snv 1.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs7156573
rs7156573
HIF1A ; HIF1A-AS3
1 14 61711103 intron variant G/A snv 0.94 0.700 1.000 1 2012 2012
dbSNP: rs7775051
rs7775051
LOC105378102
1 6 163932893 intron variant T/C snv 7.3E-02 0.700 1.000 1 2012 2012
dbSNP: rs817774
rs817774 		1 7 98511885 intergenic variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs873242
rs873242
TLL1
1 4 165943957 intron variant G/A snv 3.7E-02 0.700 1.000 1 2012 2012
dbSNP: rs9322913
rs9322913 		1 14 32900409 intergenic variant G/T snv 0.98 0.700 1.000 1 2012 2012
dbSNP: rs9689060
rs9689060 		1 6 163399936 intergenic variant C/T snv 3.8E-02 0.700 1.000 1 2012 2012
dbSNP: rs9873831
rs9873831 		1 3 103269840 intergenic variant T/C snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10504249
rs10504249
LINC01602 ; LOC105375856
3 8 57876522 intron variant A/G snv 1.7E-02 0.700 1.000 1 2013 2013
dbSNP: rs10826334
rs10826334 		3 10 59620724 intron variant C/A;G snv 0.700 1.000 1 2013 2013
dbSNP: rs10832417
rs10832417
KCNQ1 ; KCNQ1OT1
3 11 2631427 non coding transcript exon variant T/G snv 0.32 0.700 1.000 1 2013 2013
dbSNP: rs10930597
rs10930597 		3 2 173462117 intergenic variant C/T snv 0.14 0.700 1.000 1 2013 2013
dbSNP: rs11037965
rs11037965 		1 11 44356606 intergenic variant C/T snv 9.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs11867410
rs11867410
APOH
3 17 66231245 intron variant T/C snv 4.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs11887188
rs11887188 		3 2 234394166 intergenic variant C/T snv 0.11 0.700 1.000 1 2013 2013