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: rs10041756
rs10041756
1 1.000 0.040 5 22996131 intergenic variant G/A snv 0.14 0.700 1.000 1 2017 2017
dbSNP: rs10043333
rs10043333
1 1.000 0.040 5 158816761 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10043478
rs10043478
1 1.000 0.040 5 138853022 intron variant G/C snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs10046678
rs10046678
1 1.000 0.040 8 23958610 intergenic variant T/G snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs10048683
rs10048683
1 1.000 0.040 2 26097650 intron variant G/A snv 0.77 0.700 1.000 1 2017 2017
dbSNP: rs10050141
rs10050141
1 1.000 0.040 4 76530384 intron variant G/A snv 9.0E-02 0.700 1.000 1 2017 2017
dbSNP: rs10052628
rs10052628
1 1.000 0.040 5 25949752 intergenic variant C/T snv 7.8E-02 0.700 1.000 1 2017 2017
dbSNP: rs10053503
rs10053503
1 1.000 0.040 5 104778862 intron variant T/G snv 8.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs10053765
rs10053765
1 1.000 0.040 5 99658228 intergenic variant T/C snv 0.49 0.700 1.000 1 2017 2017
dbSNP: rs10054105
rs10054105
3 0.925 0.080 5 111573636 intron variant T/G snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs10054454
rs10054454
1 1.000 0.040 5 78264811 intron variant T/C snv 0.23 0.700 1.000 1 2017 2017
dbSNP: rs10057744
rs10057744
1 1.000 0.040 5 170109750 downstream gene variant C/T snv 0.89 0.700 1.000 1 2017 2017
dbSNP: rs1006066
rs1006066
1 1.000 0.040 6 17679884 intron variant G/C snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs10061629
rs10061629
1 1.000 0.040 5 77369396 intron variant C/G;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10061900
rs10061900
1 1.000 0.040 5 158826534 intron variant T/C snv 0.59 0.700 1.000 1 2017 2017
dbSNP: rs10062083
rs10062083
1 1.000 0.040 5 9130861 intron variant A/C snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs10062992
rs10062992
1 1.000 0.040 5 98143166 intron variant G/A snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs10063003
rs10063003
1 1.000 0.040 5 98143216 intron variant G/A snv 0.54 0.700 1.000 1 2017 2017
dbSNP: rs10063061
rs10063061
1 1.000 0.040 5 126608051 intron variant A/C snv 0.26 0.700 1.000 1 2017 2017
dbSNP: rs10063424
rs10063424
1 1.000 0.040 5 170108518 synonymous variant T/C snv 0.91 0.90 0.700 1.000 1 2017 2017
dbSNP: rs10064820
rs10064820
C9
1 1.000 0.040 5 39324690 intron variant G/A snv 3.1E-02 0.700 1.000 1 2017 2017
dbSNP: rs10064843
rs10064843
1 1.000 0.040 5 25948342 regulatory region variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs10067455
rs10067455
1 1.000 0.040 5 88162105 intergenic variant G/T snv 0.82 0.700 1.000 1 2017 2017
dbSNP: rs10067626
rs10067626
1 1.000 0.040 5 31914860 intron variant C/T snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs10069142
rs10069142
1 1.000 0.040 5 115777468 upstream gene variant A/G;T snv 0.700 1.000 1 2017 2017