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: rs10207567
rs10207567
ICA1L
1 2 202850250 intron variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11162351
rs11162351
AK5
1 1 77479047 intron variant C/G snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs1124694
rs1124694
LINC02752
1 11 11077129 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1145074
rs1145074
SPATA5L1
1 15 45411626 intron variant T/A;G snv 0.45 0.700 1.000 1 2018 2018
dbSNP: rs12727980
rs12727980
LINC00862
1 1 200289967 intron variant C/T snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs1276720
rs1276720
CUBN
1 10 16929427 intron variant C/T snv 0.65 0.700 1.000 1 2018 2018
dbSNP: rs146311723
rs146311723
USP3
2 1.000 0.080 15 63512308 intron variant T/C snv 0.14 0.700 1.000 1 2018 2018
dbSNP: rs17368443
rs17368443
SBF2
1 11 10275289 intron variant G/C snv 5.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs189107782
rs189107782
FRG1-DT
1 4 189807855 intron variant C/T snv 1.5E-03 0.700 1.000 1 2018 2018
dbSNP: rs2023844
rs2023844
HOTTIP
1 7 27203619 intron variant G/A snv 0.93 0.700 1.000 1 2018 2018
dbSNP: rs2338796
rs2338796
FBXL20
1 17 39399374 intron variant A/G snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs28601761
rs28601761 		13 1.000 0.040 8 125487789 intron variant C/G snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs34823645
rs34823645
C2orf83
1 2 227647210 intron variant T/C snv 3.9E-04 0.700 1.000 1 2019 2019
dbSNP: rs35483183
rs35483183
COL4A4
1 2 227011971 intron variant G/A snv 8.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs3805382
rs3805382
NMU
1 4 55605384 intron variant A/G snv 0.36 0.29 0.700 1.000 1 2018 2018
dbSNP: rs4109437
rs4109437
FRG1-DT
1 4 189848068 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs4410790
rs4410790
AHR ; LOC101927609
9 0.882 0.160 7 17244953 intron variant T/C snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs4665972
rs4665972
SNX17
9 2 27375230 intron variant T/C snv 0.69 0.700 1.000 1 2018 2018
dbSNP: rs4738817
rs4738817
CHD7
1 8 60708054 intron variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs539606836
rs539606836
CUBN
1 10 16963744 intron variant G/A snv 1.7E-04 0.700 1.000 1 2019 2019
dbSNP: rs55798132
rs55798132
LOC105377785
1 8 2808621 intron variant G/A;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6535594
rs6535594
NR3C2
2 4 148211605 intron variant G/A snv 0.54 0.700 1.000 1 2018 2018
dbSNP: rs67339103
rs67339103
LRMDA
2 10 76133928 intron variant G/A;C;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6750228
rs6750228
NRXN1 ; LOC730100
1 2 51084986 intron variant T/A snv 6.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs6768627
rs6768627
MYL3
1 3 46853886 intron variant C/T snv 0.13 0.700 1.000 1 2018 2018