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: rs7609897
rs7609897
COLQ
3 0.925 0.080 3 15461174 intron variant G/T snv 0.22 0.710 1.000 2 2017 2018
dbSNP: rs4662344
rs4662344
ARHGAP15
3 0.925 0.080 2 143591289 intron variant T/C snv 0.82 0.710 1.000 1 2017 2017
dbSNP: rs67153654
rs67153654
FAM155A
3 0.925 0.080 13 107572636 intron variant T/A;C snv 0.710 1.000 1 2017 2017
dbSNP: rs6734367
rs6734367
ARHGAP15
1 2 143556678 intron variant T/A;G snv 0.700 1.000 2 2018 2019
dbSNP: rs10120333
rs10120333
PCSK5
1 9 76125437 intron variant T/G snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs10173528
rs10173528
BABAM2
1 2 28065525 intron variant C/T snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs10471645
rs10471645
CWC27
1 5 64999536 intron variant T/C snv 0.88 0.700 1.000 1 2018 2018
dbSNP: rs10472291
rs10472291 		1 5 37772678 regulatory region variant C/A snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs115490395
rs115490395 		1 1 110120397 intergenic variant T/A snv 7.8E-03 0.700 1.000 1 2018 2018
dbSNP: rs11619840
rs11619840
FAM155A
1 13 107566610 intron variant C/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs11667256
rs11667256
SPINT2
1 19 38245164 intron variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11727676
rs11727676
HHIP
14 0.776 0.080 4 144737912 synonymous variant T/C snv 6.6E-02 6.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs11920441
rs11920441
DOCK3
1 3 51062589 intron variant T/C snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs11934833
rs11934833
LINC02272
1 4 156636431 intron variant C/G snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs12041565
rs12041565
KIF26B
1 1 245609739 intron variant C/T snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs12293535
rs12293535
CALCB
1 11 14993308 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs12531839
rs12531839
ELFN1 ; LOC105375124
1 7 1714917 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs12942267
rs12942267
ZBTB4
1 17 7469318 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs13247106
rs13247106
CALD1
1 7 134874629 intron variant A/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs1381335
rs1381335
CCN3
1 8 119415408 intron variant C/T snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs138699
rs138699
GTPBP1
1 22 38733703 intron variant G/A snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs139711468
rs139711468 		1 12 19939051 intron variant G/A snv 1.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs1427669
rs1427669
TNS1
1 2 217930633 intron variant T/G snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs148376933
rs148376933
UNC50
1 2 98612512 intron variant C/T snv 1.4E-03 0.700 1.000 1 2018 2018
dbSNP: rs1544387
rs1544387
BMPR1B
1 4 94852434 intron variant G/T snv 0.61 0.700 1.000 1 2018 2018