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: rs7057398
rs7057398
CLDN2 ; MORC4 ; RIPPLY1
5 0.827 0.080 X 106901299 intron variant T/C snv 0.41 0.710 1.000 2 2015 2018
dbSNP: rs10787903
rs10787903
EIF3A
1 1.000 0.080 10 119064457 intron variant T/C snv 0.49 0.700 1.000 1 2018 2018
dbSNP: rs11092578
rs11092578
MORC4
1 1.000 0.080 X 106983213 intron variant C/T snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs12008279
rs12008279
CLDN2 ; MORC4
3 0.882 0.080 X 106917472 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs12014762
rs12014762
MORC4
3 0.882 0.080 X 106940440 intron variant C/T snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs12688091
rs12688091
NUP62CL
1 1.000 0.080 X 107131628 intron variant G/A snv 0.23 0.700 1.000 1 2018 2018
dbSNP: rs12847061
rs12847061
PIH1D3
1 1.000 0.080 X 107230661 intron variant C/T snv 5.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs1285594
rs1285594
NUP62CL
1 1.000 0.080 X 107158099 intron variant G/C snv 0.700 1.000 1 2018 2018
dbSNP: rs138700403
rs138700403
PRSS2
1 1.000 0.080 7 142768604 intron variant A/C snv 5.2E-04 0.700 1.000 1 2018 2018
dbSNP: rs141052845
rs141052845
MORC4
1 1.000 0.080 X 106964394 intron variant A/G snv 5.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs147767607
rs147767607
PRSS2
1 1.000 0.080 7 142769934 intron variant T/C snv 0.700 1.000 1 2018 2018
dbSNP: rs148655558
rs148655558
RNF128
1 1.000 0.080 X 106768355 intron variant T/G snv 0.700 1.000 1 2018 2018
dbSNP: rs148916504
rs148916504
PRSS2
1 1.000 0.080 7 142770747 intron variant C/G snv 0.700 1.000 1 2018 2018
dbSNP: rs149055315
rs149055315
RNF128
1 1.000 0.080 X 106730962 intron variant T/A snv 5.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs17251
rs17251
TRBV27
3 0.925 0.120 7 142715462 intron variant C/A snv 0.33 0.37 0.700 1.000 1 2018 2018
dbSNP: rs2473355
rs2473355
EFHD2
1 1.000 0.080 1 15423721 intron variant A/G snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs2855983
rs2855983
PRSS2
1 1.000 0.080 7 142770582 intron variant A/G snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs34689332
rs34689332
TBC1D8B ; MORC4
1 1.000 0.080 X 106834287 intron variant G/A snv 5.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs35627987
rs35627987
PRSS2
1 1.000 0.080 7 142765664 intron variant G/T snv 3.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs4645995
rs4645995
CASP9
1 1.000 0.080 1 15522508 intron variant G/C snv 4.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs4726580
rs4726580
PRSS2 ; PRSS3P1
1 1.000 0.080 7 142762217 intron variant T/C snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs545634
rs545634
CTRC
1 1.000 0.080 1 15443607 intron variant G/A;C snv 8.9E-02; 1.6E-05 0.700 1.000 1 2018 2018
dbSNP: rs5962770
rs5962770
MORC4
1 1.000 0.080 X 106893680 intron variant T/C snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs66491909
rs66491909
RNF128
1 1.000 0.080 X 106732269 intron variant G/A snv 0.21 0.700 1.000 1 2018 2018
dbSNP: rs76047242
rs76047242
TBC1D8B ; MORC4
1 1.000 0.080 X 106816683 intron variant C/T snv 2.5E-02 0.700 1.000 1 2018 2018