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: rs9974023
rs9974023
RALY
2 20 34051022 intron variant A/C;G snv 0.700 1.000 1 2010 2010
dbSNP: rs9941751
rs9941751
TRPC4AP
2 20 35057906 intron variant A/G snv 0.14 0.700 1.000 1 2010 2010
dbSNP: rs9789510
rs9789510
MAP3K2
2 2 127379436 intron variant G/A snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs976728
rs976728 		2 20 33949546 intergenic variant C/T snv 3.5E-02 0.700 1.000 1 2010 2010
dbSNP: rs9636237
rs9636237
MAP3K2
2 2 127318446 intron variant T/C snv 0.37 0.700 1.000 1 2010 2010
dbSNP: rs945959
rs945959
EDEM2 ; MMP24-AS1-EDEM2
2 20 35147102 intron variant G/C snv 0.42 0.48 0.700 1.000 1 2010 2010
dbSNP: rs932562
rs932562
EIF6 ; FAM83C-AS1
2 20 35283507 intron variant T/C snv 0.23 0.700 1.000 1 2010 2010
dbSNP: rs9287540
rs9287540
MYO7B
2 2 127540151 intron variant T/G snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs926994
rs926994
CPNE1
2 20 35633101 intron variant G/A snv 6.7E-02 0.700 1.000 1 2010 2010
dbSNP: rs911128
rs911128
EPB41L1 ; LOC100130373
2 20 36155242 non coding transcript exon variant G/C snv 5.3E-02 5.8E-02 0.700 1.000 1 2010 2010
dbSNP: rs910870
rs910870
NCOA6 ; TP53INP2 ; LOC105372599
2 20 34705089 intron variant T/C snv 0.50 0.700 1.000 1 2010 2010
dbSNP: rs910869
rs910869
NCOA6 ; TP53INP2 ; LOC105372599
2 20 34704973 intron variant C/T snv 0.35 0.700 1.000 1 2010 2010
dbSNP: rs910398
rs910398
ZNF341-AS1
2 20 33798464 intron variant G/A;T snv 0.700 1.000 1 2010 2010
dbSNP: rs906467
rs906467
DLGAP4
2 20 36420192 intron variant T/C snv 7.6E-02 0.700 1.000 1 2010 2010
dbSNP: rs906466
rs906466
DLGAP4
2 20 36420229 intron variant G/A snv 0.22 0.700 1.000 1 2010 2010
dbSNP: rs8825
rs8825
ERGIC3
2 20 35556975 splice region variant A/G snv 0.12 0.15 0.700 1.000 1 2010 2010
dbSNP: rs882436
rs882436
FER1L4
2 20 35607349 intron variant A/C snv 0.10 0.700 1.000 1 2010 2010
dbSNP: rs867186
rs867186
PROCR ; MMP24-AS1-EDEM2
15 0.752 0.120 20 35176751 missense variant A/G snv 0.10 9.7E-02 0.800 1.000 5 2010 2017
dbSNP: rs866027
rs866027
AHCY
2 20 34286504 intron variant G/A;C snv 0.700 1.000 1 2010 2010
dbSNP: rs864702
rs864702
AHCY
2 20 34283744 intron variant A/G;T snv 0.700 1.000 1 2010 2010
dbSNP: rs843901
rs843901 		2 20 34316830 intergenic variant T/G snv 0.86 0.700 1.000 1 2010 2010
dbSNP: rs819178
rs819178
AHCY ; ASIP
2 20 34237986 intron variant A/G snv 0.12 0.700 1.000 1 2010 2010
dbSNP: rs819177
rs819177
AHCY
2 20 34276497 intron variant C/G snv 0.76 0.700 1.000 1 2010 2010
dbSNP: rs819176
rs819176
AHCY
2 20 34278038 intron variant T/A;G snv 0.700 1.000 1 2010 2010
dbSNP: rs819175
rs819175
AHCY
2 20 34278375 intron variant G/C;T snv 0.700 1.000 1 2010 2010