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: rs104895428
rs104895428
NOD2
1 1.000 0.040 16 50710953 missense variant C/G snv 0.700 0
dbSNP: rs104895429
rs104895429
NOD2
1 1.000 0.040 16 50711152 missense variant A/C;G snv 4.0E-06; 7.2E-05 0.700 0
dbSNP: rs104895431
rs104895431
NOD2
1 1.000 0.040 16 50711203 missense variant C/T snv 9.7E-04 1.0E-03 0.700 0
dbSNP: rs104895432
rs104895432
NOD2
1 1.000 0.040 16 50711232 missense variant G/A snv 3.1E-04 3.3E-04 0.700 0
dbSNP: rs104895438
rs104895438
NOD2
2 0.925 0.120 16 50711745 missense variant G/A;T snv 6.4E-04; 5.6E-05 0.700 0
dbSNP: rs104895439
rs104895439
NOD2
1 1.000 0.040 16 50711746 missense variant C/T snv 1.6E-05 0.700 0
dbSNP: rs104895440
rs104895440
NOD2
1 1.000 0.040 16 50712048 missense variant C/T snv 1.2E-05 2.1E-05 0.700 0
dbSNP: rs104895442
rs104895442
NOD2
1 1.000 0.040 16 50712184 missense variant C/T snv 1.2E-05 7.0E-06 0.700 0
dbSNP: rs104895443
rs104895443
NOD2
1 1.000 0.040 16 50712243 missense variant G/A snv 2.4E-04 2.0E-04 0.700 0
dbSNP: rs104895444
rs104895444
NOD2
1 1.000 0.040 16 50712288 missense variant G/A;T snv 1.1E-03 0.700 0
dbSNP: rs104895445
rs104895445
NOD2
1 1.000 0.040 16 50716651 missense variant G/A snv 8.0E-05 7.7E-05 0.700 0
dbSNP: rs104895446
rs104895446
NOD2
1 1.000 0.040 16 50716902 missense variant A/G snv 0.700 0
dbSNP: rs104895447
rs104895447
NOD2
1 1.000 0.040 16 50716931 missense variant A/G;T snv 1.3E-03; 4.0E-06 0.700 0
dbSNP: rs104895453
rs104895453
NOD2
1 1.000 0.040 16 50722678 missense variant G/A;T snv 6.8E-05; 4.0E-06 0.700 0
dbSNP: rs104895468
rs104895468
NOD2
1 1.000 0.040 16 50699751 missense variant G/A;T snv 2.8E-05 0.700 0
dbSNP: rs104895469
rs104895469
NOD2
1 1.000 0.040 16 50710981 missense variant A/C snv 2.4E-04 1.5E-04 0.700 0
dbSNP: rs104895470
rs104895470
NOD2
1 1.000 0.040 16 50710998 missense variant A/T snv 4.8E-05 1.4E-05 0.700 0
dbSNP: rs104895471
rs104895471
NOD2
1 1.000 0.040 16 50711559 missense variant C/G snv 0.700 0
dbSNP: rs34684955
rs34684955
NOD2
1 1.000 0.040 16 50699832 missense variant G/A snv 1.7E-03 7.1E-03 0.700 0
dbSNP: rs1217691063
rs1217691063
MTHFR
614 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 0.040 1.000 4 1999 2016
dbSNP: rs145922845
rs145922845
IL10 ; IL19
1 1.000 0.040 1 206772393 missense variant C/T snv 1.9E-03 1.8E-03 0.030 0.667 3 2000 2005
dbSNP: rs1048230
rs1048230
SLC11A2
5 0.827 0.160 12 50992283 synonymous variant A/G snv 0.17 0.15 0.010 1.000 1 2000 2000
dbSNP: rs2066844
rs2066844
NOD2
54 0.587 0.520 16 50712015 missense variant C/T snv 2.6E-02 2.9E-02 1.000 0.940 83 2001 2018
dbSNP: rs2066845
rs2066845
NOD2
46 0.611 0.600 16 50722629 missense variant G/C;T snv 1.1E-02; 2.2E-04 1.000 0.949 78 2001 2019
dbSNP: rs5743272
rs5743272
NOD2
1 1.000 0.040 16 50710966 missense variant A/G snv 9.6E-04 3.8E-03 0.710 1.000 7 2001 2018