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: rs174583
rs174583
FADS2
16 0.807 0.320 11 61842278 intron variant C/T snv 0.35 0.700 1.000 1 2011 2011
dbSNP: rs17487514
rs17487514
CHRNB4 ; RPL18P11 ; LOC112268142
3 0.925 0.080 15 78661443 non coding transcript exon variant C/T snv 0.19 0.700 1.000 1 2012 2012
dbSNP: rs1794282
rs1794282 		6 0.807 0.320 6 32698749 intergenic variant C/T snv 6.4E-02 0.700 1.000 1 2012 2012
dbSNP: rs1846594
rs1846594 		2 0.925 0.120 3 113197356 intergenic variant G/A;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1926203
rs1926203
ACTA2 ; FAS ; STAMBPL1
3 0.882 0.160 10 88967577 intron variant C/A snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs193473
rs193473
HORMAD2-AS1
1 1.000 0.080 22 30052410 intron variant A/G;T snv 0.700 1.000 1 2011 2011
dbSNP: rs1978083
rs1978083
HORMAD2
1 1.000 0.080 22 30174454 intron variant C/G snv 0.21 0.700 1.000 1 2011 2011
dbSNP: rs200426271
rs200426271
MTMR3
1 1.000 0.080 22 29948468 intron variant -/G ins 0.700 1.000 1 2011 2011
dbSNP: rs2017677
rs2017677
MTMR3
1 1.000 0.080 22 29987273 non coding transcript exon variant G/C;T snv 0.700 1.000 1 2011 2011
dbSNP: rs2023683
rs2023683
HORMAD2 ; LOC105372988
1 1.000 0.080 22 30203607 intron variant G/A snv 0.22 0.700 1.000 1 2011 2011
dbSNP: rs2051764
rs2051764
MTMR3
2 0.925 0.080 22 29965892 intron variant G/A;C snv 0.74 0.700 1.000 1 2011 2011
dbSNP: rs2233956
rs2233956
C6orf15 ; PSORS1C1
5 0.827 0.320 6 31113428 upstream gene variant T/C snv 0.12 0.700 1.000 1 2012 2012
dbSNP: rs2256543
rs2256543
HLA-A
2 0.925 0.080 6 29970056 downstream gene variant T/C snv 0.59 0.700 1.000 1 2009 2009
dbSNP: rs2257914
rs2257914
TRIM10
2 0.925 0.200 6 30152786 3 prime UTR variant C/A snv 0.17 0.700 1.000 1 2011 2011
dbSNP: rs2412963
rs2412963
MTMR3
1 1.000 0.080 22 29995292 non coding transcript exon variant G/A snv 0.74 0.700 1.000 1 2011 2011
dbSNP: rs2508049
rs2508049
LOC105375010
1 1.000 0.080 6 29856106 intron variant A/G snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs2517598
rs2517598
TRIM31 ; TRIM31-AS1
4 0.851 0.280 6 30112497 synonymous variant G/A snv 0.14 0.13 0.700 1.000 1 2012 2012
dbSNP: rs2523987
rs2523987
TRIM31 ; TRIM31-AS1
5 0.827 0.280 6 30112216 intron variant A/C snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs2523989
rs2523989
TRIM31 ; TRIM31-AS1
5 0.827 0.280 6 30110498 missense variant C/T snv 0.12 0.12 0.700 1.000 1 2012 2012
dbSNP: rs2535238
rs2535238
ZFP57
1 1.000 0.080 6 29677261 5 prime UTR variant C/A;T snv 0.700 1.000 1 2012 2012
dbSNP: rs2596571
rs2596571 		2 0.925 0.160 6 31380245 upstream gene variant G/C snv 0.74 0.700 1.000 1 2011 2011
dbSNP: rs2596573
rs2596573 		1 1.000 0.080 6 31380153 upstream gene variant C/T snv 0.75 0.700 1.000 1 2011 2011
dbSNP: rs259919
rs259919
ZNRD1ASP
6 0.882 0.080 6 30057726 intron variant G/A snv 0.25 0.700 1.000 1 2012 2012
dbSNP: rs259940
rs259940
ZNRD1ASP
2 0.925 0.080 6 30044157 intron variant A/G snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs2656069
rs2656069
IREB2
5 0.882 0.080 15 78453365 intron variant C/G;T snv 0.700 1.000 1 2012 2012