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: rs10189761
rs10189761 		4 0.882 0.120 2 646364 intergenic variant T/A snv 0.82 0.010 1.000 1 2019 2019
dbSNP: rs10423928
rs10423928
GIPR
12 0.807 0.200 19 45679046 intron variant T/A snv 0.19 0.010 1.000 1 2019 2019
dbSNP: rs11006544
rs11006544
LOC107984235
3 1.000 0.040 10 59510886 intergenic variant T/C snv 7.3E-03 0.700 1.000 1 2019 2019
dbSNP: rs11110004
rs11110004
ANKS1B
3 1.000 0.040 12 99694540 intron variant T/C snv 5.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs112434206
rs112434206 		3 1.000 0.040 5 33083283 intron variant A/C;G snv 7.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs113235453
rs113235453
NUBPL
3 1.000 0.040 14 31849939 intron variant A/G snv 3.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs1136201
rs1136201
ERBB2
34 0.645 0.280 17 39723335 missense variant A/G;T snv 0.20 0.010 1.000 1 2019 2019
dbSNP: rs114821210
rs114821210 		3 1.000 0.040 5 166089843 intergenic variant C/A snv 6.0E-03 0.700 1.000 1 2019 2019
dbSNP: rs12362161
rs12362161 		3 1.000 0.040 11 98834502 intergenic variant C/A;G snv 0.700 1.000 1 2019 2019
dbSNP: rs139130723
rs139130723 		3 1.000 0.040 6 14411553 intergenic variant A/G snv 4.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs140226130
rs140226130
CCDC178
8 0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 0.010 1.000 1 2019 2019
dbSNP: rs142803096
rs142803096 		3 1.000 0.040 6 14420151 intergenic variant G/C snv 4.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs144303414
rs144303414 		3 1.000 0.040 18 48509413 intergenic variant A/C snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs148133894
rs148133894 		3 1.000 0.040 16 24584678 intergenic variant T/C snv 2.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs149322277
rs149322277
CA5A
3 1.000 0.040 16 87925065 intron variant C/T snv 5.6E-03 0.700 1.000 1 2019 2019
dbSNP: rs149447933
rs149447933
LOC101928331 ; LOC105374942
3 1.000 0.040 6 14453908 intron variant C/G snv 4.4E-03 0.700 1.000 1 2019 2019
dbSNP: rs150109621
rs150109621
CELSR1
3 1.000 0.040 22 46429532 intron variant C/T snv 5.9E-03 0.700 1.000 1 2019 2019
dbSNP: rs150381023
rs150381023
CELSR1
3 1.000 0.040 22 46423108 intron variant T/C snv 5.8E-03 0.700 1.000 1 2019 2019
dbSNP: rs16917667
rs16917667
C8orf37-AS1
3 1.000 0.040 8 95439600 intron variant G/A snv 4.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs1695
rs1695
GSTP1
188 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 0.010 1.000 1 2019 2019
dbSNP: rs1700575
rs1700575
LOC105374647
3 1.000 0.040 5 8543925 intron variant A/T snv 0.26 0.700 1.000 1 2019 2019
dbSNP: rs1800437
rs1800437
GIPR
13 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 0.010 1.000 1 2019 2019
dbSNP: rs1801282
rs1801282
PPARG
131 0.500 0.840 3 12351626 missense variant C/G snv 0.11 8.9E-02 0.010 < 0.001 1 2019 2019
dbSNP: rs1805192
rs1805192
PPARG
121 0.510 0.840 3 12379739 missense variant C/G snv 0.010 < 0.001 1 2019 2019
dbSNP: rs188344082
rs188344082 		3 1.000 0.040 1 18783262 intergenic variant G/A snv 1.8E-02 0.700 1.000 1 2019 2019