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: 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: 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: rs11214775
rs11214775
HTR3B
1 1.000 0.080 11 113936459 intron variant G/A snv 0.29 0.700 1.000 2 2014 2018
dbSNP: rs2659124
rs2659124
LOC105372441
1 1.000 0.080 19 50851341 upstream gene variant A/T snv 0.84 0.700 1.000 2 2015 2019
dbSNP: rs2807031
rs2807031
XAGE3
1 1.000 0.080 X 52867918 intron variant T/C snv 0.18 0.700 1.000 2 2014 2018
dbSNP: rs4713266
rs4713266
NEDD9
1 1.000 0.080 6 11218797 intron variant C/T snv 0.43 0.700 1.000 2 2014 2018
dbSNP: rs4844289
rs4844289
LOC107985688
1 1.000 0.080 X 71188133 intron variant A/G snv 0.51 0.700 1.000 2 2014 2018
dbSNP: rs76934034
rs76934034
MARCHF8
1 1.000 0.080 10 45587537 intron variant T/C snv 5.7E-02 0.700 1.000 2 2014 2018
dbSNP: rs80130819
rs80130819
LOC105369750
1 1.000 0.080 12 48025835 upstream gene variant A/C;G snv 0.700 1.000 2 2014 2018
dbSNP: rs8014671
rs8014671
LOC101928075
1 1.000 0.080 14 70625539 intron variant G/A snv 0.46 0.700 1.000 2 2014 2018
dbSNP: rs9287719
rs9287719
NOL10
1 1.000 0.080 2 10570604 downstream gene variant C/T snv 0.60 0.700 1.000 2 2014 2018
dbSNP: rs1004030
rs1004030
MMP14
1 1.000 0.080 14 22836440 upstream gene variant T/C snv 0.39 0.700 1.000 1 2018 2018
dbSNP: rs10122495
rs10122495
UBAP2
1 1.000 0.080 9 34049781 upstream gene variant T/A snv 0.73 0.700 1.000 1 2018 2018
dbSNP: rs1016342
rs1016342
PCAT1 ; PRNCR1 ; CASC19 ; PCAT2
1 1.000 0.080 8 127080210 non coding transcript exon variant C/G;T snv 0.700 1.000 1 2007 2007
dbSNP: rs1031588
rs1031588
PCAT1 ; PRNCR1 ; CASC19 ; PCAT2
1 1.000 0.080 8 127081032 non coding transcript exon variant C/A snv 0.24 0.700 1.000 1 2007 2007
dbSNP: rs1041449
rs1041449 		1 1.000 0.080 21 41529494 intron variant A/G snv 0.42 0.700 1.000 1 2014 2014
dbSNP: rs10460109
rs10460109 		1 1.000 0.080 18 75324210 intergenic variant T/C snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs1048169
rs1048169
HAUS6
1 1.000 0.080 9 19055967 3 prime UTR variant T/C snv 0.46 0.700 1.000 1 2018 2018
dbSNP: rs10763567
rs10763567 		1 1.000 0.080 10 46057653 regulatory region variant G/A;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10774740
rs10774740 		1 1.000 0.080 12 114228397 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs10793821
rs10793821 		1 1.000 0.080 5 134500518 upstream gene variant C/A;T snv 0.62 0.700 1.000 1 2018 2018
dbSNP: rs10845938
rs10845938 		1 1.000 0.080 12 14263984 intergenic variant A/G snv 0.52 0.700 1.000 1 2018 2018
dbSNP: rs11125927
rs11125927 		1 1.000 0.080 2 62525840 regulatory region variant G/A snv 0.86 0.700 1.000 1 2019 2019
dbSNP: rs111599055
rs111599055
FBRSL1
1 1.000 0.080 12 132563775 intron variant A/C;G snv 0.700 1.000 1 2018 2018