Source: GWASCAT ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1333037
CDKN2B-AS1
0.925 0.040 9 22040766 intron variant C/T snv 0.71 2
rs1333040
CDKN2B-AS1
0.732 0.280 9 22083405 intron variant C/G;T snv 2
rs1333042
CDKN2B-AS1
0.827 0.120 9 22103814 intron variant A/G snv 0.63 2
rs1440581
PPM1K-DT
1.000 0.080 4 88305270 intron variant T/A;C snv 2
rs1481805 1.000 0.080 8 71121190 intron variant A/T snv 0.58 2
rs1532002
LRP1B
1.000 0.080 2 140292500 intron variant G/A snv 2.3E-02 2
rs16879003
ATXN1
1.000 0.080 6 16745008 intron variant T/C;G snv 2
rs17214144
OSBPL3
1.000 0.080 7 24846128 intron variant T/C snv 0.20 2
rs1912826
KLKB1
4 186228386 intron variant G/A;C snv 2
rs2680830
VSNL1
1.000 0.080 2 17596817 intron variant A/G;T snv 0.94 2
rs2891168
CDKN2B-AS1
0.851 0.160 9 22098620 intron variant A/G snv 0.40 2
rs4272321
PTPRN2
1.000 0.080 7 158159143 intron variant A/G snv 4.6E-04 2
rs448792
FRY
1.000 0.080 13 32103287 intron variant T/A;C snv 2
rs543554
FRY
1.000 0.080 13 32127501 intron variant A/G;T snv 2
rs59490629
PDSS2
1.000 0.080 6 107256268 intron variant G/A snv 8.5E-02 2
rs59811240
MTSS1
1.000 0.080 8 124709787 intron variant C/A snv 1.3E-02 2
rs6606859
GABRG3
1.000 0.080 15 27032254 intron variant C/A;T snv 2
rs6898559
ALDH7A1
1.000 0.080 5 126557237 intron variant G/A snv 0.66 2
rs72928364
ABI3BP
1.000 0.080 3 100894935 intron variant C/T snv 0.39 2
rs7442201
NSG1
1.000 0.080 4 4360022 intron variant A/C;G snv 2
rs74570061
ARL9
1.000 0.080 4 56517605 intron variant T/C snv 3.9E-02 2
rs75629841
MTSS1
1.000 0.080 8 124714135 intron variant G/A;T snv 2
rs76294234 1.000 0.080 4 83241025 intron variant A/G snv 1.5E-02 2
rs77757620
STARD9
1.000 0.080 15 42661399 intron variant C/T snv 3.8E-02 2
rs77934287 1.000 0.080 12 23071319 intron variant A/G;T snv 2