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: rs56214552
rs56214552
TRIQK
2 1.000 0.080 8 93011994 intron variant T/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs9004
rs9004
ZNF7 ; COMMD5
1 8 144842937 stop gained C/G;T snv 1.6E-05; 0.31 0.700 1.000 1 2018 2018
dbSNP: rs117905930
rs117905930 		2 1.000 0.080 9 88973603 intron variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs56353579
rs56353579
GOLM1
1 9 86078634 intron variant G/A snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs6479525
rs6479525
LINC01508
2 1.000 0.080 9 90331096 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs12268753
rs12268753
PRKG1
1 10 52058389 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11237982
rs11237982 		2 1.000 0.080 11 79730650 intergenic variant T/C snv 0.18 0.700 1.000 1 2015 2015
dbSNP: rs12295181
rs12295181
HBE1 ; HBG2
1 11 5270506 intron variant C/T snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs148410317
rs148410317
IFITM10
1 11 1749985 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11177782
rs11177782
BEST3 ; LOC105369823
1 12 69662005 intron variant C/T snv 1.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs35551159
rs35551159 		1 12 60075450 intergenic variant C/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs4762194
rs4762194 		1 12 97789941 intergenic variant G/A snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs56186534
rs56186534
LOC105369949
1 12 104410836 regulatory region variant G/C snv 5.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs1449587
rs1449587 		1 13 48839332 regulatory region variant C/T snv 0.31 0.700 1.000 1 2017 2017
dbSNP: rs4942792
rs4942792
PDS5B
1 13 32663326 intron variant C/A;G snv 0.700 1.000 1 2018 2018
dbSNP: rs9528384
rs9528384 		1 13 61728432 regulatory region variant A/G snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs117609474
rs117609474
LINC02331
1 14 53804550 intron variant A/G snv 1.0E-02 0.700 1.000 1 2018 2018
dbSNP: rs12436690
rs12436690 		1 14 97119552 intron variant G/A snv 0.12 0.700 1.000 1 2013 2013
dbSNP: rs6571943
rs6571943
LOC105370461
1 14 39556042 intron variant C/T snv 0.77 0.700 1.000 1 2017 2017
dbSNP: rs147828834
rs147828834
FSIP1
1 15 39602982 intron variant A/T snv 8.3E-03 0.700 1.000 1 2018 2018
dbSNP: rs150900094
rs150900094 		1 15 87284961 intergenic variant A/C snv 2.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs4776997
rs4776997 		1 15 67858585 intron variant A/G;T snv 0.77 0.700 1.000 1 2015 2015
dbSNP: rs61751117
rs61751117
RAB11A ; DENND4A
1 15 65741731 synonymous variant A/C snv 2.6E-02 2.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs11074779
rs11074779 		1 16 26440122 intergenic variant T/C snv 0.16 0.700 1.000 1 2015 2015
dbSNP: rs113338984
rs113338984
SNTB2
1 16 69282015 intron variant C/A;T snv 0.700 1.000 1 2018 2018