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: rs116046250
rs116046250
GABRG3
1 1.000 0.040 15 26986803 intron variant T/G snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs192876988
rs192876988
LOC105377300
4 0.851 0.120 4 79376097 intergenic variant T/C snv 1.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs37792
rs37792 		1 1.000 0.040 5 53348817 intergenic variant G/A snv 0.67 0.700 1.000 1 2019 2019
dbSNP: rs57403204
rs57403204 		1 1.000 0.040 X 141990766 intron variant A/G snv 3.7E-02 0.700 1.000 1 2019 2019
dbSNP: rs66459581
rs66459581
PRPSAP1
1 1.000 0.040 17 76359184 intron variant C/- del 0.11 0.700 1.000 1 2019 2019
dbSNP: rs79079890
rs79079890
LOC105376360 ; LOC107984193
1 1.000 0.040 10 3641956 intergenic variant T/G snv 0.10 0.700 1.000 1 2019 2019
dbSNP: rs10069690
rs10069690
TERT
53 0.595 0.560 5 1279675 intron variant C/T snv 0.36 0.700 1.000 1 2017 2017
dbSNP: rs10962692
rs10962692 		3 0.925 0.120 9 16915876 upstream gene variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs11651755
rs11651755
HNF1B
9 0.763 0.160 17 37739849 intron variant T/C snv 0.52 0.700 1.000 1 2017 2017
dbSNP: rs13113999
rs13113999 		1 1.000 0.040 4 166265894 intergenic variant T/G snv 0.35 0.700 1.000 1 2017 2017
dbSNP: rs1400482
rs1400482
LINC00824
2 0.925 0.120 8 128529685 intron variant G/A snv 0.13 0.700 1.000 1 2017 2017
dbSNP: rs144962376
rs144962376
MLLT10
2 0.925 0.120 10 21589903 intron variant CCCCTT/-;CCCCTTCCCCTT delins 0.700 1.000 1 2017 2017
dbSNP: rs150293538
rs150293538
LINC01111
1 1.000 0.040 8 76408119 intron variant C/T snv 1.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs1879586
rs1879586
PLEKHM1
2 0.925 0.120 17 45489971 intron variant C/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs2165109
rs2165109
ACOXL ; MIR4435-2HG
2 0.925 0.120 2 111061081 intron variant A/C snv 0.25 0.700 1.000 1 2017 2017
dbSNP: rs58722170
rs58722170
RSPO1
2 0.925 0.120 1 37630749 intron variant G/C snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs6005807
rs6005807
TTC28 ; LOC101929594
2 0.925 0.120 22 28538325 intron variant T/C snv 0.89 0.700 1.000 1 2017 2017
dbSNP: rs62274041
rs62274041 		3 0.925 0.120 3 156717851 upstream gene variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs6755777
rs6755777
HAGLR ; HAGLROS
3 0.882 0.120 2 176178498 non coding transcript exon variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs711830
rs711830
HOXD3 ; HAGLR
3 0.882 0.120 2 176172583 3 prime UTR variant A/C;G;T snv 0.76 0.700 1.000 1 2017 2017
dbSNP: rs7207826
rs7207826
SKAP1
2 0.925 0.120 17 48423311 intron variant T/C snv 0.33 0.700 1.000 1 2017 2017
dbSNP: rs7405776
rs7405776
HNF1B
6 0.807 0.120 17 37733029 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs7705526
rs7705526
TERT
15 0.776 0.240 5 1285859 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs7902587
rs7902587 		2 0.925 0.080 10 103934543 intergenic variant C/T snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs7953249
rs7953249
HNF1A-AS1
4 0.882 0.160 12 120965921 splice region variant G/A snv 0.59 0.700 1.000 1 2017 2017