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: rs12258967
rs12258967
CACNB2
5 10 18439030 intron variant C/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs12940887
rs12940887
ZNF652
5 17 49325445 intron variant C/T snv 0.28 0.700 1.000 1 2011 2011
dbSNP: rs13082711
rs13082711 		5 3 27496418 intergenic variant T/C snv 0.16 0.700 1.000 1 2011 2011
dbSNP: rs1378942
rs1378942
CSK
16 0.790 0.240 15 74785026 intron variant C/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs198846
rs198846
H1-6
7 6 26107235 downstream gene variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2782980
rs2782980
LOC105378492
4 10 114021768 regulatory region variant T/C snv 0.66 0.700 1.000 1 2011 2011
dbSNP: rs319690
rs319690
MAP4
4 3 47885994 intron variant T/C snv 0.39 0.700 1.000 1 2011 2011
dbSNP: rs381815
rs381815
PLEKHA7
6 1.000 0.040 11 16880721 intron variant C/A;T snv 0.24 0.700 1.000 1 2011 2011
dbSNP: rs419076
rs419076
MECOM
6 3 169383098 intron variant T/A;C snv 0.700 1.000 1 2011 2011
dbSNP: rs4590817
rs4590817
CABCOCO1
5 10 61707795 intron variant G/C snv 0.15 0.700 1.000 1 2011 2011
dbSNP: rs6015450
rs6015450
ZNF831
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 1 2011 2011
dbSNP: rs9313772
rs9313772
LINC02227
2 5 158377449 intron variant C/T snv 0.30 0.700 1.000 1 2011 2011
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