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: rs10195263
rs10195263 		1 2 150869278 intergenic variant G/A;C snv 0.800 1.000 1 2012 2012
dbSNP: rs10517025
rs10517025
ATP8A1
1 4 42451236 intron variant C/T snv 0.15 0.800 1.000 1 2012 2012
dbSNP: rs11034653
rs11034653
LOC105376634
1 11 38267043 intergenic variant C/T snv 9.1E-02 0.800 1.000 1 2012 2012
dbSNP: rs11171846
rs11171846
TIMELESS
1 12 56434272 intron variant C/T snv 6.4E-02 0.800 1.000 1 2012 2012
dbSNP: rs11242417
rs11242417
GFRA3
2 1.000 0.040 5 138263645 intron variant T/G snv 0.13 0.800 1.000 1 2012 2012
dbSNP: rs12044963
rs12044963
KCND3
2 1.000 0.080 1 111849738 intron variant G/T snv 0.10 0.800 1.000 1 2012 2012
dbSNP: rs13067593
rs13067593
LPP
1 3 188866891 intron variant A/G snv 0.12 0.800 1.000 1 2012 2012
dbSNP: rs13181561
rs13181561
SMIM33
1 5 139471320 intron variant G/A snv 0.61 0.800 1.000 1 2012 2012
dbSNP: rs1516489
rs1516489
LOC105374276
1 3 191804063 intergenic variant A/C snv 8.8E-02 0.800 1.000 1 2012 2012
dbSNP: rs1540283
rs1540283
PHEX
1 X 22129934 intron variant C/G;T snv 0.800 1.000 1 2012 2012
dbSNP: rs1584468
rs1584468
PRR16
1 5 120601996 intron variant G/A snv 9.6E-02 0.800 1.000 1 2012 2012
dbSNP: rs17007761
rs17007761 		1 2 122468047 intron variant C/A snv 6.0E-02 0.800 1.000 1 2012 2012
dbSNP: rs17142462
rs17142462 		1 7 119966578 intergenic variant C/A;T snv 0.800 1.000 1 2012 2012
dbSNP: rs17221323
rs17221323
DIP2C
1 10 572745 intron variant T/C snv 0.13 0.800 1.000 1 2012 2012
dbSNP: rs17252936
rs17252936
MAMLD1
1 X 150467029 intron variant A/G snv 0.11 0.800 1.000 1 2012 2012
dbSNP: rs17290760
rs17290760
NDUFB6 ; SMIM27
1 9 32556382 intron variant A/G snv 0.10 0.800 1.000 1 2012 2012
dbSNP: rs17299841
rs17299841
LOC112267973
1 6 127700658 intergenic variant A/C snv 6.4E-02 0.800 1.000 1 2012 2012
dbSNP: rs17444059
rs17444059
PDE4D
1 5 59264891 intron variant T/C snv 8.5E-02 0.800 1.000 1 2012 2012
dbSNP: rs17714988
rs17714988
LINC00381
1 13 74421523 intron variant A/G snv 5.7E-02 0.800 1.000 1 2012 2012
dbSNP: rs2043599
rs2043599 		1 19 55939683 intergenic variant A/G snv 5.9E-02 0.800 1.000 1 2012 2012
dbSNP: rs2048161
rs2048161
ZNF827
1 4 145932013 intron variant A/C;G snv 0.800 1.000 1 2012 2012
dbSNP: rs210359
rs210359
LINC02331 ; LOC105370504
1 14 53700754 intron variant A/C snv 0.95 0.800 1.000 1 2012 2012
dbSNP: rs2255327
rs2255327
BLK
1 8 11552483 intron variant C/T snv 1.2E-02 0.800 1.000 1 2012 2012
dbSNP: rs2272205
rs2272205
COL4A4
1 2 227051208 intron variant T/C snv 9.1E-02 7.7E-02 0.800 1.000 1 2012 2012
dbSNP: rs2501276
rs2501276
CDC42 ; CDC42-AS1
1 1 22047131 intron variant C/T snv 8.1E-02 0.800 1.000 1 2012 2012