Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs11959928
DAB2 ; C9
1.000 0.080 5 39397030 intron variant T/A snv 0.39 4
rs12460876
SLC7A9
1.000 0.080 19 32865985 intron variant T/C snv 0.36 4
rs174530
MYRF ; TMEM258
1.000 0.080 11 61779120 non coding transcript exon variant A/G snv 0.30 4
rs174564
FADS2 ; FADS1
1.000 0.080 11 61820833 intron variant A/G snv 0.30 4
rs174567
FADS1 ; FADS2
1.000 0.080 11 61825533 intron variant A/G;T snv 4
rs174568
FADS1 ; FADS2
1.000 0.080 11 61826344 missense variant C/A;T snv 0.37 4
rs174580
FADS2
1.000 0.080 11 61839170 intron variant A/C;G snv 4
rs174592
FADS2
1.000 0.080 11 61851136 intron variant A/G snv 0.44 4
rs187355703
HOXD-AS2 ; LOC100129455 ; HOXD8
1.000 0.080 2 176128855 intron variant C/G snv 1.5E-02 1.5E-02 4
rs2279463
SLC22A2
1.000 0.080 6 160247357 intron variant A/G;T snv 4
rs2453533 1.000 0.080 15 45349027 intergenic variant C/A snv 0.56 4
rs2467853
SPATA5L1
1.000 0.080 15 45406595 intron variant T/A;G snv 4
rs347685
TFDP2
1.000 0.080 3 142088295 intron variant C/A snv 0.74 4
rs4744712
PIP5K1B
1.000 0.080 9 68819791 intron variant A/C;T snv 4
rs491567
WDR72
1.000 0.080 15 53654396 intron variant A/C snv 0.34 4
rs515299
CFH
0.925 0.080 1 196737547 missense variant G/A;C;T snv 4.8E-05; 1.7E-02 4
rs6431731
LINC01804
1.000 0.080 2 15722878 intron variant C/T snv 0.97 4
rs6465825 1.000 0.080 7 77787122 downstream gene variant T/C snv 0.41 4
rs7123489 1.000 0.080 11 65756781 intron variant C/A snv 0.29 4
rs73728279
PRKAG2
1.000 0.080 7 151714408 intron variant G/A;T snv 4
rs80282103
LARP4B
1.000 0.080 10 853131 intron variant A/T snv 0.12 4
rs867394500
ACE
0.851 0.080 17 63477301 missense variant G/T snv 4
rs102274
TMEM258
1.000 0.080 11 61790354 non coding transcript exon variant T/C snv 0.28 3
rs1044261
GTPBP4 ; IDI2
1.000 0.080 10 1019770 stop gained C/T snv 5.0E-02 6.0E-02 3
rs1077989
GPHN ; TMEM229B
1.000 0.080 14 67509105 intron variant A/C snv 0.39 3