Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6774721 1.000 0.040 3 49344465 upstream gene variant G/A snv 0.15 4
rs7107356 1.000 0.040 11 47654618 downstream gene variant A/G snv 0.45 4
rs754593
MAPT
1.000 0.040 17 45977330 non coding transcript exon variant G/A snv 0.52 4
rs8089865
DCC
1.000 0.040 18 53431552 intron variant G/A;C snv 4
rs10965780 1.000 0.040 9 23341717 intron variant C/G;T snv 3
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs138472420
BICRA
1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs141746753 1.000 0.040 8 56934154 intergenic variant C/T snv 3.1E-03 3
rs150175932
DCLK2
1.000 0.040 4 150101495 intron variant T/C snv 1.6E-02 3
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 3
rs1994321 1.000 0.040 11 12065766 upstream gene variant G/T snv 0.33 3
rs34467936 1.000 0.040 11 47893747 intergenic variant A/G snv 0.30 3
rs34668726
KLHL29
1.000 0.040 2 23673031 intron variant C/G snv 0.13 3
rs35825582
ARHGAP15
1.000 0.040 2 143491193 intron variant G/A snv 0.45 3
rs35863382
PPP4R3A
1.000 0.040 14 91472532 intron variant C/T snv 6.0E-02 3
rs3843954 1.000 0.040 13 57974377 intergenic variant G/A;C snv 3
rs4800995
LOC105372130
1.000 0.040 18 55748146 intron variant G/A snv 0.76 3
rs599550
TCF4
1.000 0.040 18 55585157 intron variant G/A;T snv 3
rs61572747 1.000 0.040 17 45383525 regulatory region variant A/G snv 0.25 3
rs7104036
RAPSN
1.000 0.040 11 47440589 intron variant A/G snv 0.31 3
rs7212450
LOC105371490
1.000 0.040 17 2688646 intron variant G/A;C snv 3
rs73720034 1.000 0.040 7 125794995 intergenic variant T/C snv 7.2E-02 3