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: rs10864462
rs10864462
PEX14
1 1 10552101 intron variant A/T snv 0.11 0.700 1.000 1 2019 2019
dbSNP: rs10882899
rs10882899
FRAT2 ; LOC105378448
1 10 97336188 intron variant G/C snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs10899789
rs10899789
LINC02633 ; LOC105378271
1 10 43322411 upstream gene variant C/G snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs10956401
rs10956401
PVT1
1 8 127990173 non coding transcript exon variant G/A snv 0.31 0.700 1.000 1 2019 2019
dbSNP: rs10980457
rs10980457
SVEP1
1 9 110576455 intron variant A/C snv 9.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs10982456
rs10982456
TNFSF8 ; DELEC1
1 9 114928478 intron variant T/C snv 0.57 0.700 1.000 1 2019 2019
dbSNP: rs1099448
rs1099448
TNFSF4 ; LOC100506023
1 1 173262759 intergenic variant C/T snv 0.58 0.700 1.000 1 2019 2019
dbSNP: rs11010134
rs11010134
LINC02634
1 10 35229101 intron variant A/G snv 0.29 0.700 1.000 1 2019 2019
dbSNP: rs11014291
rs11014291
PRTFDC1
1 10 24909758 intron variant T/C snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs11055989
rs11055989
ATF7IP
1 12 14469068 intron variant A/G snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs1105935
rs1105935
KIAA2012
1 2 202161307 intron variant T/A;C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs11068852
rs11068852
TCHP
1 12 109904616 intron variant T/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11077961
rs11077961 		1 17 83054873 upstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11084096
rs11084096
SIGLEC5
1 19 51625542 intron variant G/A snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs1109151
rs1109151
ZC3H7B
1 22 41356940 intron variant A/G snv 0.42 0.700 1.000 1 2019 2019
dbSNP: rs11106430
rs11106430
LINC01619
1 12 92118652 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs111286706
rs111286706
TMEM116
1 12 111955882 intron variant C/A snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs11150152
rs11150152
MAF
1 16 79315586 regulatory region variant T/C snv 0.59 0.700 1.000 1 2019 2019
dbSNP: rs111526888
rs111526888 		1 18 60304392 downstream gene variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11164971
rs11164971 		1 1 91576688 regulatory region variant T/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs111678372
rs111678372 		1 5 36087768 intergenic variant C/T snv 1.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs11185551
rs11185551
PIGX ; NRROS
1 3 196641320 intron variant G/C snv 0.14 0.700 1.000 1 2019 2019
dbSNP: rs111955202
rs111955202
MAP4K4
1 2 101788512 intron variant A/G snv 1.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs112069438
rs112069438
TXNDC11
1 16 11733034 intron variant G/A snv 2.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs112180833
rs112180833
LINC01081
1 16 86258762 intron variant G/C snv 6.7E-03 0.700 1.000 1 2019 2019