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: rs1015164
rs1015164
8 0.925 3 46410189 intron variant A/C;G;T snv 0.700 1.000 2 2015 2019
dbSNP: rs10484554
rs10484554
11 0.807 0.200 6 31306778 intron variant C/T snv 0.12 0.700 1.000 2 2009 2010
dbSNP: rs10947207
rs10947207
5 1.000 6 31393708 downstream gene variant T/C snv 0.31 0.700 1.000 2 2009 2010
dbSNP: rs12153855
rs12153855
11 0.776 0.320 6 32107027 intron variant T/C snv 0.11 0.700 1.000 2 2009 2010
dbSNP: rs12191877
rs12191877
7 0.851 0.120 6 31285148 intron variant C/T snv 0.12 0.700 1.000 2 2009 2010
dbSNP: rs13198118
rs13198118
4 1.000 6 30802955 intron variant T/G snv 0.17 0.700 1.000 2 2009 2010
dbSNP: rs13199524
rs13199524
9 0.807 0.240 6 32098988 intron variant C/T snv 8.4E-02 0.700 1.000 2 2009 2010
dbSNP: rs13210132
rs13210132
4 1.000 6 31033366 intron variant A/G snv 4.3E-02 0.700 1.000 2 2009 2010
dbSNP: rs13437082
rs13437082
7 1.000 6 31386783 upstream gene variant C/T snv 0.32 0.700 1.000 2 2009 2010
dbSNP: rs17207190
rs17207190
4 1.000 6 31601743 intergenic variant G/A;T snv 2.8E-02 0.700 1.000 2 2009 2010
dbSNP: rs2249742
rs2249742
7 0.925 0.120 6 31272944 intron variant C/T snv 0.50 0.700 1.000 2 2009 2010
dbSNP: rs2284178
rs2284178
6 0.925 0.120 6 31464348 non coding transcript exon variant C/T snv 0.44 0.700 1.000 2 2009 2010
dbSNP: rs2516513
rs2516513
5 0.925 0.120 6 31479811 downstream gene variant C/T snv 0.20 0.700 1.000 2 2009 2010
dbSNP: rs2524123
rs2524123
5 0.925 0.040 6 31297537 intron variant T/C snv 0.34 0.700 1.000 2 2009 2010
dbSNP: rs2844509
rs2844509
6 0.882 0.160 6 31543147 intron variant A/G snv 0.23 0.700 1.000 2 2009 2010
dbSNP: rs28732144
rs28732144
4 1.000 6 31588428 non coding transcript exon variant G/A snv 2.8E-02 0.700 1.000 2 2009 2010
dbSNP: rs2894207
rs2894207
8 0.882 0.160 6 31295974 intron variant T/C snv 0.20 0.700 1.000 2 2009 2010
dbSNP: rs3093661
rs3093661
TNF
4 1.000 6 31575981 intron variant G/A snv 3.5E-02 0.700 1.000 2 2009 2010
dbSNP: rs3093662
rs3093662
TNF
9 0.851 0.200 6 31576412 intron variant A/G snv 7.1E-02 0.700 1.000 2 2009 2010
dbSNP: rs3094212
rs3094212
5 1.000 6 31117993 non coding transcript exon variant G/A snv 0.58 0.700 1.000 2 2009 2010
dbSNP: rs3095320
rs3095320
4 1.000 6 31120157 intron variant G/A;C snv 0.700 1.000 2 2009 2010
dbSNP: rs3130424
rs3130424
5 0.925 0.040 6 31250462 intergenic variant A/C;G;T snv 0.700 1.000 2 2009 2010
dbSNP: rs3130473
rs3130473
6 0.882 0.160 6 31231431 intergenic variant C/T snv 0.23 0.700 1.000 2 2009 2010
dbSNP: rs3130981
rs3130981
5 0.925 0.080 6 31116036 missense variant T/C;G snv 0.76 0.700 1.000 2 2009 2010
dbSNP: rs3134899
rs3134899
4 1.000 6 31505509 intron variant C/T snv 0.80 0.700 1.000 2 2009 2010