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: rs11558471
rs11558471
SLC30A8 ; LOC105375716
5 1.000 0.080 8 117173494 3 prime UTR variant A/G snv 0.25 0.800 1.000 2 2011 2013
dbSNP: rs11603334
rs11603334
ARAP1
5 1.000 0.080 11 72721940 5 prime UTR variant G/A snv 0.12 0.800 1.000 2 2011 2013
dbSNP: rs6235
rs6235
PCSK1 ; LOC101929710
8 0.925 0.120 5 96393194 missense variant C/G snv 0.26 0.23 0.800 1.000 2 2011 2013
dbSNP: rs10501320
rs10501320
MADD ; MADD-AS1
5 0.925 0.120 11 47272248 5 prime UTR variant G/C snv 0.17 0.800 1.000 1 2011 2011
dbSNP: rs10838687
rs10838687
MADD
2 11 47291341 intron variant T/G snv 0.31 0.800 1.000 1 2011 2011
dbSNP: rs1549318
rs1549318 		1 15 70816808 intergenic variant C/T snv 0.55 0.800 1.000 1 2011 2011
dbSNP: rs4502156
rs4502156 		4 1.000 0.080 15 62090956 intergenic variant T/C snv 0.55 0.800 1.000 1 2011 2011
dbSNP: rs4790333
rs4790333
SGSM2
1 17 2359409 intron variant C/A;T snv 0.44 0.800 1.000 1 2011 2011
dbSNP: rs7903146
rs7903146
TCF7L2
93 0.554 0.680 10 112998590 intron variant C/G;T snv 0.800 1.000 1 2011 2011
dbSNP: rs9727115
rs9727115
SNX7
1 1 98711697 intron variant G/A snv 0.37 0.800 1.000 1 2011 2011
dbSNP: rs1051006
rs1051006
MADD
2 11 47285034 missense variant G/A;C snv 0.26; 4.0E-06 0.700 1.000 1 2013 2013
dbSNP: rs10830963
rs10830963
MTNR1B
27 0.776 0.400 11 92975544 intron variant C/G snv 0.22 0.700 1.000 1 2014 2014
dbSNP: rs11185790
rs11185790
PANK1
3 10 89612776 intron variant G/A snv 0.15 0.700 1.000 1 2009 2009
dbSNP: rs150781447
rs150781447
TBC1D30
1 12 64830440 missense variant C/T snv 5.4E-03 5.3E-03 0.700 1.000 1 2013 2013
dbSNP: rs1800437
rs1800437
GIPR
13 0.827 0.160 19 45678134 missense variant G/C snv 0.18 0.17 0.700 1.000 1 2017 2017
dbSNP: rs2943641
rs2943641 		18 0.763 0.160 2 226229029 intergenic variant T/C snv 0.67 0.700 1.000 1 2017 2017
dbSNP: rs35233100
rs35233100
MADD
1 11 47285079 stop gained C/T snv 3.8E-02 3.9E-02 0.700 1.000 1 2013 2013
dbSNP: rs3824420
rs3824420
KANK1
1 9 712766 missense variant G/A;C snv 3.8E-02; 1.2E-05 0.700 1.000 1 2013 2013
dbSNP: rs5015480
rs5015480 		9 0.851 0.120 10 92705802 downstream gene variant C/T snv 0.42 0.700 1.000 1 2017 2017
dbSNP: rs61741902
rs61741902
SGSM2
1 17 2379485 missense variant G/A snv 1.0E-02 9.1E-03 0.700 1.000 1 2013 2013
dbSNP: rs6930337
rs6930337
SASH1
1 6 148466870 intron variant C/G;T snv 0.700 1.000 1 2008 2008
dbSNP: rs7172432
rs7172432 		4 0.925 0.080 15 62104190 intergenic variant A/G snv 0.51 0.700 1.000 1 2013 2013
dbSNP: rs742642
rs742642
CDKAL1
3 1.000 0.080 6 20664850 intron variant G/A snv 0.21 0.700 1.000 1 2014 2014
dbSNP: rs7944584
rs7944584
MADD
5 1.000 0.080 11 47314769 intron variant A/T snv 0.19 0.700 1.000 1 2013 2013
dbSNP: rs933360
rs933360
GRB10
2 7 50690548 intron variant C/T snv 0.60 0.700 1.000 1 2014 2014