Source: GWASCAT ×
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: rs1058024
rs1058024
NUP50 ; LOC105373064
1 1.000 0.040 22 45186979 3 prime UTR variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs11089940
rs11089940
IGLV10-54
1 1.000 0.040 22 22155065 intron variant G/A snv 5.5E-02 0.700 1.000 1 2017 2017
dbSNP: rs11090584
rs11090584 		1 1.000 0.040 22 29853358 intergenic variant T/A;C snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs11705386
rs11705386 		1 1.000 0.040 22 27638385 regulatory region variant C/T snv 3.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs11913192
rs11913192 		1 1.000 0.040 22 48447383 upstream gene variant G/A snv 8.3E-02 0.700 1.000 1 2017 2017
dbSNP: rs12165516
rs12165516
LOC284930
1 1.000 0.040 22 47783584 intron variant A/G snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs12484281
rs12484281
MYO18B
1 1.000 0.040 22 25787450 intron variant T/C snv 0.22 0.700 1.000 1 2017 2017
dbSNP: rs12627929
rs12627929
MTMR3 ; MIR6818
1 1.000 0.040 22 30005238 non coding transcript exon variant A/G snv 9.4E-03 0.700 1.000 1 2017 2017
dbSNP: rs12628523
rs12628523
MYO18B
1 1.000 0.040 22 25788238 intron variant T/C snv 2.6E-02 0.700 1.000 1 2017 2017
dbSNP: rs13053400
rs13053400
CECR2
1 1.000 0.040 22 17523132 intron variant G/A snv 5.4E-02 0.700 1.000 1 2017 2017
dbSNP: rs132834
rs132834
NUP50-DT
1 1.000 0.040 22 45158316 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs132873
rs132873
NUP50 ; LOC112267891
1 1.000 0.040 22 45170821 intron variant C/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs132875
rs132875
NUP50 ; LOC112267891
1 1.000 0.040 22 45171031 5 prime UTR variant C/A;G snv 0.21 0.700 1.000 1 2017 2017
dbSNP: rs132881
rs132881
NUP50 ; LOC112267891
1 1.000 0.040 22 45171699 non coding transcript exon variant C/A snv 0.21 0.20 0.700 1.000 1 2017 2017
dbSNP: rs132883
rs132883
NUP50 ; LOC112267891
1 1.000 0.040 22 45172630 intron variant G/T snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs132884
rs132884
NUP50 ; LOC112267891
1 1.000 0.040 22 45173105 intron variant A/G snv 0.20 0.700 1.000 1 2017 2017
dbSNP: rs134009
rs134009 		1 1.000 0.040 22 27638589 regulatory region variant G/A snv 0.11 0.700 1.000 1 2017 2017
dbSNP: rs134743
rs134743 		1 1.000 0.040 22 26135950 intergenic variant A/T snv 0.24 0.700 1.000 1 2017 2017
dbSNP: rs134748
rs134748
LOC102724801
1 1.000 0.040 22 26147321 intergenic variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs138517
rs138517
GRAMD4
1 1.000 0.040 22 46610615 intron variant G/A snv 0.79 0.700 1.000 1 2017 2017
dbSNP: rs138521
rs138521
GRAMD4
1 1.000 0.040 22 46610350 intron variant G/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs16980756
rs16980756
MYO18B
1 1.000 0.040 22 25798974 intron variant C/T snv 0.27 0.700 1.000 1 2017 2017
dbSNP: rs16981470
rs16981470
SEZ6L
1 1.000 0.040 22 26181380 intron variant C/T snv 0.12 0.700 1.000 1 2017 2017
dbSNP: rs16985231
rs16985231 		1 1.000 0.040 22 27641723 regulatory region variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs16985255
rs16985255 		1 1.000 0.040 22 27645916 intergenic variant A/G snv 3.0E-02 0.700 1.000 1 2017 2017