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: rs113111175
rs113111175
PPP6R2
2 22 50429282 intron variant C/T snv 7.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs1978968
rs1978968
MICAL3
3 22 17965347 intron variant C/T snv 0.17 0.700 1.000 1 2019 2019
dbSNP: rs4822108
rs4822108
TCF20
1 22 42309864 intron variant C/A snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs535842
rs535842
LINC01638
1 22 27225190 upstream gene variant G/A snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs6001508
rs6001508 		1 22 39221697 downstream gene variant C/A snv 0.34 0.700 1.000 1 2019 2019
dbSNP: rs6006399
rs6006399
HORMAD2 ; LOC105372988
1 22 30202527 intron variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs9680696
rs9680696
MICAL3
1 22 17935399 intron variant C/T snv 0.19 0.700 1.000 1 2019 2019
dbSNP: rs1041733
rs1041733 		1 21 34311960 intron variant T/A snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs13615
rs13615
ADAMTS1
1 21 26837348 3 prime UTR variant A/G snv 9.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs2823118
rs2823118 		1 21 15173586 intergenic variant A/T snv 0.53 0.700 1.000 1 2019 2019
dbSNP: rs2834591
rs2834591
CLIC6
1 21 34698903 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4818281
rs4818281 		1 21 16749208 intergenic variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7283798
rs7283798
KCNJ6 ; DSCR4
1 21 38034828 intron variant A/T snv 0.18 0.700 1.000 1 2019 2019
dbSNP: rs143384
rs143384
GDF5
17 0.827 0.200 20 35437976 5 prime UTR variant G/A snv 0.44 0.700 1.000 2 2019 2019
dbSNP: rs4809221
rs4809221
SLC2A4RG
2 20 63741353 non coding transcript exon variant G/A;C;T snv 0.69; 3.2E-05 0.700 1.000 2 2019 2019
dbSNP: rs1000972
rs1000972 		2 20 6641070 regulatory region variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11086748
rs11086748 		1 20 39379415 intergenic variant T/A;G snv 0.46 0.700 1.000 1 2019 2019
dbSNP: rs12481092
rs12481092 		3 20 46858178 upstream gene variant C/T snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs13044825
rs13044825 		1 20 46865179 upstream gene variant G/C snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs2145272
rs2145272 		8 20 6645571 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2179687
rs2179687
SLX4IP
2 20 10633647 intron variant A/G snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs2236519
rs2236519
EYA2 ; LOC101927355
2 20 46900932 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2326420
rs2326420 		1 20 4078510 upstream gene variant G/A snv 0.70 0.700 1.000 1 2019 2019
dbSNP: rs2426338
rs2426338
ATP9A
1 20 51646224 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6037062
rs6037062
ENTPD6
1 20 25222256 non coding transcript exon variant G/A snv 0.53 0.700 1.000 1 2019 2019