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: rs1448903
rs1448903
ADAM23
1 2 206444237 intron variant A/G snv 6.1E-02 0.700 1.000 3 2018 2019
dbSNP: rs6136
rs6136
SELP
17 0.752 0.440 1 169594713 missense variant T/G snv 8.2E-02 7.5E-02 0.700 1.000 3 2018 2018
dbSNP: rs7412
rs7412
APOE
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 3 2018 2018
dbSNP: rs1018454
rs1018454
DPT
1 1 168728523 intron variant A/C snv 0.57 0.700 1.000 2 2018 2018
dbSNP: rs10405357
rs10405357
LILRB5
1 19 54255803 intron variant T/C snv 0.50 0.700 1.000 2 2018 2018
dbSNP: rs1048328
rs1048328
KLK11
1 19 51024108 missense variant G/A;C snv 6.0E-02; 4.2E-06 0.700 1.000 2 2018 2018
dbSNP: rs10490666
rs10490666
VIT
1 2 36705350 intron variant A/T snv 0.26 0.700 1.000 2 2018 2018
dbSNP: rs1050239
rs1050239
SMPD1
1 11 6394233 missense variant G/A;C snv 0.19 0.700 1.000 2 2018 2019
dbSNP: rs10509554
rs10509554
LIPN
1 10 88766035 intron variant C/T snv 0.26 0.700 1.000 2 2018 2018
dbSNP: rs111577916
rs111577916 		1 11 126201454 downstream gene variant G/A;T snv 0.700 1.000 2 2018 2018
dbSNP: rs112433249
rs112433249
IMPAD1
1 8 56964017 missense variant T/C snv 1.0E-02 9.1E-03 0.700 1.000 2 2018 2018
dbSNP: rs1126477
rs1126477
LTF
7 0.807 0.200 3 46459778 missense variant C/T snv 0.34 0.53 0.700 1.000 2 2018 2018
dbSNP: rs1147707
rs1147707
FSTL1
1 3 120450401 intron variant C/T snv 0.28 0.700 1.000 2 2018 2018
dbSNP: rs11555096
rs11555096
FAH
2 1.000 15 80180184 missense variant C/A;T snv 1.7E-02 0.700 1.000 2 2018 2018
dbSNP: rs11558819
rs11558819
ICOSLG
1 21 44236891 missense variant C/T snv 0.27 0.700 1.000 2 2018 2018
dbSNP: rs115668827
rs115668827 		1 1 107135646 upstream gene variant G/C snv 3.2E-02 0.700 1.000 2 2018 2018
dbSNP: rs11581248
rs11581248
SLAMF7
1 1 160750284 intron variant C/T snv 8.7E-02 8.6E-02 0.700 1.000 2 2018 2018
dbSNP: rs12599777
rs12599777
NAGPA ; NAGPA-AS1
1 16 5029465 non coding transcript exon variant A/G snv 0.17 0.700 1.000 2 2018 2018
dbSNP: rs12740374
rs12740374
CELSR2
16 0.851 0.040 1 109274968 3 prime UTR variant G/T snv 0.22 0.700 1.000 2 2018 2018
dbSNP: rs12964
rs12964
VAMP1 ; TAPBPL
2 12 6463025 3 prime UTR variant T/C snv 0.46 0.700 1.000 2 2018 2018
dbSNP: rs13318853
rs13318853
CPB1
1 3 148844612 intron variant G/A;T snv 0.22; 4.0E-06 0.700 1.000 2 2018 2018
dbSNP: rs138616686
rs138616686
NQO2
1 6 3003736 5 prime UTR variant A/C;G snv 0.700 1.000 2 2018 2018
dbSNP: rs139695917
rs139695917
GXYLT1
1 12 42133239 intron variant T/C snv 7.8E-03 0.700 1.000 2 2018 2018
dbSNP: rs1468810
rs1468810
VIT
1 2 36766797 intron variant C/A snv 0.45 0.700 1.000 2 2018 2018
dbSNP: rs15881
rs15881
GFRA2
1 8 21693256 3 prime UTR variant A/C;G;T snv 0.48; 1.2E-05 0.700 1.000 2 2018 2018