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: rs4522104
rs4522104 		1 10 98127275 intergenic variant A/C snv 0.15 0.700 1.000 1 2012 2012
dbSNP: rs1861090
rs1861090 		1 12 9777083 intergenic variant A/G snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs10844706
rs10844706
CD69
1 12 9757536 intron variant C/A snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs10844639
rs10844639 		1 12 9736166 upstream gene variant C/T snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs1455587
rs1455587
RAB31 ; LOC105371981
1 18 9710557 intron variant G/T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs3909451
rs3909451
LNPEP
1 5 96959417 intron variant G/T snv 0.40 0.700 1.000 1 2012 2012
dbSNP: rs10844372
rs10844372 		1 12 9663306 upstream gene variant G/C snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs1891536
rs1891536
ENTPD1 ; ENTPD1-AS1
1 10 95831540 intron variant T/C snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs10076188
rs10076188
MCTP1 ; SLF1
1 5 94726834 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs13535
rs13535
ZNF559 ; ZNF559-ZNF177
1 19 9343497 3 prime UTR variant A/G snv 0.61 0.700 1.000 1 2012 2012
dbSNP: rs7517538
rs7517538 		1 1 9272644 downstream gene variant T/C snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs9932566
rs9932566 		1 16 9124844 downstream gene variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs3540
rs3540
IQGAP1
2 15 90502176 3 prime UTR variant G/A snv 0.43 0.700 1.000 1 2016 2016
dbSNP: rs72928038
rs72928038
BACH2
19 0.695 0.360 6 90267049 intron variant G/A snv 0.11 0.700 1.000 1 2016 2016
dbSNP: rs3775121
rs3775121
GAK
1 4 899732 intron variant G/A snv 0.33 0.700 1.000 1 2012 2012
dbSNP: rs2146338
rs2146338
LRRC8C ; LOC101927952 ; LOC107985743
1 1 89755569 intron variant C/T snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs382745
rs382745
SPG7
1 16 89537178 3 prime UTR variant A/G snv 0.47 0.700 1.000 1 2012 2012
dbSNP: rs10777181
rs10777181
POC1B
1 12 89514850 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10554589
rs10554589
ANKRD11 ; LOC105371414
1 16 89295870 intron variant ATGTG/- delins 0.83 0.700 1.000 1 2016 2016
dbSNP: rs2150820
rs2150820
PM20D2
1 6 89163257 3 prime UTR variant C/T snv 0.37 0.700 1.000 1 2012 2012
dbSNP: rs142550358
rs142550358 		5 9 88777772 intron variant CT/- delins 3.9E-02 0.700 1.000 1 2016 2016
dbSNP: rs4414876
rs4414876
CGGBP1 ; ZNF654
1 3 88133918 intron variant A/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs272500
rs272500
ODF2L
1 1 86361950 intron variant A/G;T snv 0.700 1.000 1 2012 2012
dbSNP: rs1883932
rs1883932
PLCB1 ; LOC105372521
2 20 8628941 intron variant A/T snv 0.58 0.700 1.000 1 2016 2016
dbSNP: rs311581
rs311581
POLR1A
1 2 86055837 intron variant A/G;T snv 0.700 1.000 1 2012 2012