Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs12127701
MYBPHL
1 109295642 intron variant A/G snv 6.2E-02 4
rs11264339 1.000 0.040 1 155168172 downstream gene variant C/T snv 0.56 2
rs111724808 1 22411453 intergenic variant T/G snv 3.1E-02 1
rs2503715
FAAP20
1 2212668 non coding transcript exon variant A/G snv 0.89 1
rs397637
OBSCN
1 228265627 intron variant G/T snv 0.27 1
rs4648819
SKI
1 2273351 intron variant G/A snv 0.91 1
rs75013985
KCND3
1 111987808 intron variant A/G snv 6.6E-03 1
rs7538988 1 51351869 downstream gene variant T/C snv 2.2E-02 1
rs6730558
LOC105373411
2 8616053 intron variant C/T snv 0.47 5
rs11897119
MEIS1
2 66544868 intron variant T/A;C snv 3
rs882300
LOC107985947
1.000 0.080 2 136218685 intergenic variant T/C;G snv 3
rs10865355
MEIS1
2 66537865 intron variant A/G snv 0.61 1
rs11677371
MEIS1
2 66529281 intron variant A/G;T snv 1
rs13018106 2 163518692 intergenic variant G/C snv 0.43 1
rs17026148
LOC101929667 ; SLC8A1
2 40530430 intron variant G/A snv 9.1E-02 1
rs17026156
SLC8A1 ; LOC101929667
2 40533825 intron variant T/C snv 6.8E-02 1
rs2732860
TMEM182
2 102781875 intron variant G/A snv 0.55 1
rs3856447
LOC105373411
2 8610136 intron variant A/G snv 0.44 1
rs3891585
MEIS1
2 66529844 intron variant A/C;G snv 1
rs4430933
MEIS1
2 66522478 intron variant A/G snv 0.58 1
rs4433986
MEIS1
2 66533179 intron variant A/G snv 0.59 1
rs4952632
LOC101929667 ; SLC8A1
2 40520865 intron variant T/G snv 8.5E-02 1
rs56988800
DYSF
2 71460988 intron variant C/A snv 2.7E-02 1
rs6724747
MEIS1
2 66522696 intron variant G/A snv 0.23 1
rs7603236
MEIS1
2 66535279 intron variant C/T snv 0.61 1