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: rs10054105
rs10054105
STARD4-AS1
3 0.925 0.080 5 111573636 intron variant T/G snv 0.17 0.700 1.000 1 2018 2018
dbSNP: rs10786938
rs10786938 		1 1.000 0.040 10 106280012 intergenic variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11084596
rs11084596 		3 1.000 0.040 19 31614073 regulatory region variant T/C snv 0.35 0.700 1.000 1 2018 2018
dbSNP: rs11199879
rs11199879 		3 1.000 0.040 10 121285698 regulatory region variant T/C snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs11651052
rs11651052
HNF1B
7 0.851 0.200 17 37742390 intron variant G/A snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs141179786
rs141179786 		1 1.000 0.040 18 53662174 intergenic variant A/G;T snv 2.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs148678804
rs148678804 		2 1.000 0.040 10 22138360 intergenic variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1638703
rs1638703
DLEU1
2 1.000 0.040 13 50514220 intron variant G/C snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs17144046
rs17144046 		4 0.882 0.120 10 8564051 intergenic variant A/G snv 0.28 0.700 1.000 1 2017 2017
dbSNP: rs200383755
rs200383755
GATA5
3 0.925 0.080 20 62475466 missense variant G/C snv 3.4E-03 3.0E-03 0.700 1.000 1 2018 2018
dbSNP: rs200476
rs200476 		2 1.000 0.040 6 27800570 intergenic variant A/T snv 0.28 0.700 1.000 1 2018 2018
dbSNP: rs2555019
rs2555019 		3 1.000 0.040 12 114230813 intergenic variant T/C;G snv 0.700 1.000 1 2018 2018
dbSNP: rs2556378
rs2556378
BCL11A
3 1.000 0.040 2 60535367 3 prime UTR variant T/G snv 0.81 0.700 1.000 1 2018 2018
dbSNP: rs2710383
rs2710383
SYN3
1 1.000 0.040 22 32554983 intron variant G/C snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs2853677
rs2853677
TERT
19 0.724 0.240 5 1287079 3 prime UTR variant G/A snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs2981575
rs2981575
FGFR2
4 0.882 0.120 10 121586602 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs36067435
rs36067435
ELOVL6
1 1.000 0.040 4 110180390 intron variant -/TTAT delins 0.700 1.000 1 2019 2019
dbSNP: rs381949
rs381949
CLPTM1L
3 1.000 0.040 5 1322353 intron variant G/A snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs4239633
rs4239633
UNC13A
4 0.851 0.240 19 17631660 intron variant C/T snv 0.32 0.700 1.000 1 2019 2019
dbSNP: rs4548546
rs4548546
WDR11
3 1.000 0.040 10 120870067 intron variant C/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs534957
rs534957
GCLC
1 1.000 0.040 6 53541553 intron variant G/C snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs6061244
rs6061244
GATA5
2 1.000 0.040 20 62466597 intron variant G/A;C snv 1.3E-03; 0.38 0.700 1.000 1 2018 2018
dbSNP: rs6078585
rs6078585 		1 1.000 0.040 20 12447612 intergenic variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6561599
rs6561599
DLEU1 ; RNASEH2B-AS1
2 1.000 0.040 13 50904782 non coding transcript exon variant C/G snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs677394
rs677394
C5orf66
2 1.000 0.040 5 135271869 intron variant G/C;T snv 0.700 1.000 1 2018 2018