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: rs9650622
rs9650622 		2 8 9946782 intergenic variant G/T snv 0.40 0.700 1.000 1 2018 2018
dbSNP: rs13271489
rs13271489 		2 8 9946202 intergenic variant T/C snv 0.38 0.700 1.000 1 2018 2018
dbSNP: rs187821766
rs187821766
STK3
3 8 98729050 intron variant C/T snv 3.5E-03 0.700 1.000 1 2017 2017
dbSNP: rs186208701
rs186208701
STK3
3 8 98567888 intron variant T/C snv 3.3E-03 0.700 1.000 1 2017 2017
dbSNP: rs4841235
rs4841235 		2 8 9825848 intergenic variant A/G snv 0.56 0.700 1.000 1 2018 2018
dbSNP: rs55868514
rs55868514 		2 8 9822890 intergenic variant T/C snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs187222839
rs187222839 		1 11 98073424 intergenic variant T/C snv 1.6E-03 0.700 1.000 1 2017 2017
dbSNP: rs9286060
rs9286060 		2 8 9795635 intergenic variant A/C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs11599481
rs11599481
CRTAC1
2 10 97880706 intron variant C/T snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs4851462
rs4851462
ZAP70
1 2 97740700 downstream gene variant T/C snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs4910498
rs4910498
SWAP70
4 11 9743956 intron variant A/T snv 0.61 0.700 1.000 1 2018 2018
dbSNP: rs2649044
rs2649044
SWAP70
4 11 9742422 intron variant C/T snv 0.55 0.700 1.000 2 2017 2018
dbSNP: rs360153
rs360153
SWAP70
1 11 9740727 non coding transcript exon variant T/C snv 0.57 0.700 1.000 1 2018 2018
dbSNP: rs55684003
rs55684003
MBNL2
1 13 97336435 intron variant A/G snv 0.22 0.700 1.000 1 2018 2018
dbSNP: rs360158
rs360158
SWAP70
2 11 9732054 intron variant G/A snv 0.66 0.700 1.000 1 2017 2017
dbSNP: rs7902871
rs7902871
SLIT1
2 10 97049946 intron variant A/G snv 0.21 0.700 1.000 1 2013 2013
dbSNP: rs1947228
rs1947228 		1 7 96832337 regulatory region variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs7599598
rs7599598
FER1L5
2 2 96686103 missense variant A/G;T snv 0.41 0.700 1.000 3 2017 2018
dbSNP: rs35410524
rs35410524
UFL1-AS1
2 6 96437529 intron variant C/T snv 0.15 0.700 1.000 1 2017 2017
dbSNP: rs1081707
rs1081707 		1 2 96381261 downstream gene variant G/A snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs7134060
rs7134060
CDK17
1 12 96323317 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs772178
rs772178
SNRNP200
1 2 96297946 intron variant A/C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs4984497
rs4984497
LOC105369212 ; LOC112268156
1 15 96092670 intron variant T/C snv 0.76 0.700 1.000 1 2017 2017
dbSNP: rs4984496
rs4984496
LOC105369212 ; LOC112268156
1 15 96092669 intron variant T/G snv 0.76 0.700 1.000 1 2017 2017
dbSNP: rs2579519
rs2579519
FAHD2CP
1 2 96009418 upstream gene variant T/C snv 0.37 0.700 1.000 1 2017 2017