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: rs12535041
rs12535041
ZNF804B
1 7 88944157 intron variant A/C snv 3.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs12580543
rs12580543
C1S ; LPCAT3 ; EMG1
1 12 6992881 intron variant A/C snv 0.12 0.700 1.000 1 2015 2015
dbSNP: rs16838623
rs16838623
CHRM3
2 1 239648090 intron variant A/C snv 3.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs2391388
rs2391388
ALG14
2 1 95020269 intron variant A/C snv 0.49 0.700 1.000 1 2013 2013
dbSNP: rs6671200
rs6671200
TLCD4-RWDD3 ; LOC101928118
2 1 95231973 intron variant A/C snv 0.90 0.700 1.000 1 2013 2013
dbSNP: rs6683451
rs6683451
ERVMER61-1 ; LINC01036
1 1 187323476 intron variant A/C snv 7.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs727761
rs727761
LOC101928893
1 4 78738511 regulatory region variant A/C snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs9315681
rs9315681
LHFPL6
1 13 39409534 intron variant A/C snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs10518201
rs10518201
LOC101928893
1 4 78730706 regulatory region variant A/G snv 6.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs11038755
rs11038755
PHF21A
1 11 46057150 intron variant A/G snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs11190604
rs11190604
HIF1AN
2 10 100542700 intron variant A/G snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs12098564
rs12098564
LINC01519
2 10 85193571 non coding transcript exon variant A/G snv 7.4E-02 0.700 1.000 1 2013 2013
dbSNP: rs12648219
rs12648219
LOC101928893
1 4 78734132 regulatory region variant A/G snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs12703118
rs12703118
NUB1
1 7 151345197 intron variant A/G snv 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs13361131
rs13361131
MYO10
1 5 16804871 intron variant A/G snv 6.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs1468510
rs1468510
NUB1
1 7 151360599 3 prime UTR variant A/G snv 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs16850871
rs16850871
GALNT2
1 1 230083723 intron variant A/G snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs17074093
rs17074093
DLEU1
1 13 50314567 intron variant A/G snv 5.8E-02 0.700 1.000 1 2018 2018
dbSNP: rs17648246
rs17648246
LOC107984619
2 13 44919746 intergenic variant A/G snv 5.0E-02 0.700 1.000 1 2013 2013
dbSNP: rs17651415
rs17651415
MYO10
1 5 16858112 intron variant A/G snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs727760
rs727760
LOC101928893
1 4 78738610 regulatory region variant A/G snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs7439893
rs7439893
LOC101928893
1 4 78738019 regulatory region variant A/G snv 9.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs77164426
rs77164426 		2 2 146756888 intergenic variant A/G snv 1.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs9566421
rs9566421
LHFPL6
1 13 39406692 intron variant A/G snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs9566425
rs9566425
LHFPL6
1 13 39408007 intron variant A/G snv 0.28 0.700 1.000 1 2018 2018