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: rs62113212
rs62113212
KLK3
2 0.925 0.080 19 50857584 non coding transcript exon variant C/G;T snv 0.710 0.500 2 2011 2015
dbSNP: rs7153648
rs7153648
SIX1
2 0.925 0.080 14 60655808 intron variant C/A;G snv 0.710 1.000 2 2014 2018
dbSNP: rs7210100
rs7210100
ZNF652 ; LOC102724596
2 0.925 0.080 17 49359387 intron variant G/A;C snv 0.710 1.000 2 2011 2015
dbSNP: rs721048
rs721048
EHBP1
4 0.851 0.200 2 62904596 intron variant G/A snv 0.13 0.710 1.000 2 2008 2018
dbSNP: rs12791447
rs12791447
PPFIBP2
2 0.925 0.080 11 7535346 intron variant A/G snv 6.6E-02 0.710 1.000 1 2015 2015
dbSNP: rs138708
rs138708
SUN2
2 0.925 0.080 22 38742327 missense variant G/A;T snv 2.2E-02; 4.0E-06 0.710 1.000 1 2019 2019
dbSNP: rs4646284
rs4646284
SLC22A1
2 0.925 0.080 6 160160511 downstream gene variant -/G delins 0.31 0.710 1.000 1 2015 2015
dbSNP: rs4775302
rs4775302 		2 0.925 0.080 15 46347610 intron variant G/A snv 0.49 0.710 1.000 1 2011 2011
dbSNP: rs58262369
rs58262369
ESR2
2 0.925 0.080 14 64227194 3 prime UTR variant C/T snv 2.4E-02 0.710 1.000 1 2015 2015
dbSNP: rs72725854
rs72725854
PCAT1
2 0.925 0.080 8 127062570 intron variant A/G;T snv 0.710 1.000 1 2018 2018
dbSNP: rs73862213
rs73862213
GATA2-AS1
2 0.925 0.080 3 128498656 intron variant A/G snv 8.3E-02 0.710 1.000 1 2019 2019
dbSNP: rs77911174
rs77911174
ZMIZ1 ; ZMIZ1-AS1
2 0.925 0.080 10 79067076 intron variant A/G snv 5.4E-02 0.710 1.000 1 2019 2019
dbSNP: rs78943174
rs78943174
NAALADL2
2 0.925 0.080 3 175534948 intron variant C/G;T snv 0.710 1.000 1 2015 2015
dbSNP: rs817826
rs817826 		2 0.925 0.080 9 107394019 intergenic variant C/T snv 0.81 0.710 1.000 1 2012 2012
dbSNP: rs1016343
rs1016343
PCAT1 ; PRNCR1 ; CASC19 ; PCAT2
8 0.807 0.240 8 127081052 non coding transcript exon variant C/T snv 0.20 0.700 1.000 4 2007 2015
dbSNP: rs5759167
rs5759167 		4 0.851 0.160 22 43104206 TF binding site variant G/T snv 0.40 0.700 1.000 4 2009 2018
dbSNP: rs10187424
rs10187424
VAMP8
2 0.925 0.080 2 85567174 intron variant T/A;C snv 0.700 1.000 3 2011 2018
dbSNP: rs10875943
rs10875943 		2 0.925 0.080 12 49282227 intergenic variant T/A;C snv 0.700 1.000 3 2011 2018
dbSNP: rs17599629
rs17599629
GOLPH3L
1 1.000 0.080 1 150685811 intron variant A/G snv 0.17 0.700 1.000 3 2014 2018
dbSNP: rs4242384
rs4242384 		3 0.882 0.160 8 127506309 regulatory region variant C/A snv 0.88 0.700 1.000 3 2008 2011
dbSNP: rs6465657
rs6465657
LMTK2
7 0.807 0.280 7 98187015 intron variant C/T snv 0.41 0.37 0.700 1.000 3 2008 2018
dbSNP: rs10009409
rs10009409
LOC105377273 ; LOC107986286
1 1.000 0.080 4 72989536 intergenic variant C/T snv 0.35 0.700 1.000 2 2014 2018
dbSNP: rs10086908
rs10086908
PCAT1 ; LOC105375751
1 1.000 0.080 8 126999692 intron variant T/C snv 0.28 0.700 1.000 2 2015 2019
dbSNP: rs10934853
rs10934853
EEFSEC
3 0.882 0.160 3 128319530 intron variant C/A snv 0.43 0.700 1.000 2 2009 2018
dbSNP: rs10936632
rs10936632 		2 0.925 0.080 3 170412314 intron variant C/A snv 0.41 0.700 1.000 2 2011 2018