Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1126616
SPP1
0.827 0.280 4 87982701 synonymous variant C/G;T snv 0.32 0.26 8
rs1131012
PECAM1
0.763 0.280 17 64350416 missense variant T/C snv 0.38 10
rs11320420
MYRF ; TMEM258
1.000 0.080 11 61774535 intron variant AAAAA/-;AAA;AAAA;AAAAAA delins 0.30 2
rs1156619081
UCP3
11 74005787 missense variant T/C snv 4.0E-06 1
rs11575542
FIGNL1 ; DDC
7 50463289 missense variant C/T snv 2.3E-02 5.5E-02 1
rs11662622 1.000 0.080 18 65592400 intergenic variant A/G snv 0.20 2
rs1168357
GRIP1
12 66356099 intron variant T/C snv 0.50 1
rs1171614
SLC16A9
0.882 0.200 10 59709780 5 prime UTR variant T/C snv 0.79 7
rs1171616
SLC16A9
0.882 0.200 10 59708831 intron variant G/T snv 0.79 6
rs11739136
KCNIP1 ; KCNMB1
0.827 0.200 5 170383792 missense variant C/T snv 9.9E-02 8.7E-02 10
rs117935223
PRODH
1.000 0.080 22 18923820 non coding transcript exon variant C/A snv 2
rs11864909
PDILT
0.851 0.160 16 20389517 intron variant C/T snv 0.23 7
rs11959928
DAB2 ; C9
1.000 0.080 5 39397030 intron variant T/A snv 0.39 4
rs12107
MYH9
1.000 0.040 22 36281936 3 prime UTR variant G/A;T snv 3
rs12124078
DNAJC16
1 15543404 intron variant A/G snv 0.32 3
rs12134854
SLC44A5
1.000 0.080 1 75671921 intron variant T/C snv 0.27 2
rs1217691063
MTHFR
0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs121917832
GPR19 ; CDKN1B
0.925 0.200 12 12718066 stop gained G/A snv 3
rs12194000
SLC22A16
1.000 0.080 6 110454809 intron variant A/G;T snv 2
rs1222213359
VEGFA
0.574 0.720 6 43770966 missense variant G/A snv 62
rs12313273
ORAI1
0.882 0.160 12 121625105 upstream gene variant T/C snv 0.23 4
rs1232013698
TNF
6 31577208 missense variant G/T snv 4.1E-06 1
rs12373237
LAMA3
0.851 0.200 18 23845972 intron variant G/A snv 0.47 5
rs1242780
PTPRN2
1.000 0.080 7 157757146 intron variant T/G snv 0.25 2
rs12460876
SLC7A9
1.000 0.080 19 32865985 intron variant T/C snv 0.36 4