Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 3
rs34177316
LOC107986273 ; APBB2
0.925 0.040 4 40985283 intron variant A/-;AA;AAA delins 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
rs4800995
LOC105372130
1.000 0.040 18 55748146 intron variant G/A snv 0.76 3
rs4839421
CYMP
0.925 0.040 1 110479338 intron variant C/A snv 0.40 3
rs599550
TCF4
1.000 0.040 18 55585157 intron variant G/A;T snv 3
rs6063349
CSE1L
0.925 0.040 20 49065345 intron variant G/A;C;T snv 3
rs6546604 0.925 0.040 2 70415675 intron variant G/A;T snv 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
rs73425402
NAV3
0.925 0.040 12 77503518 intron variant T/A snv 4.1E-02 3
rs73788091
FSTL4 ; MIR1289-2
1.000 0.040 5 133429517 intron variant C/T snv 0.10 3
rs77945277
BAZ1A
0.925 0.040 14 34840969 intron variant A/G snv 4.9E-03 3
rs80278479
TFAP2D
0.925 0.040 6 50758466 intron variant C/G snv 3.0E-03 3
rs10144845
YLPM1
1.000 0.040 14 74771067 intron variant C/T snv 0.62 2
rs10156548 1.000 0.040 9 23318435 intron variant G/C;T snv 2
rs10429537 1.000 0.040 9 23346844 intron variant C/G snv 0.33 2
rs10950393
TMEM106B
1.000 0.040 7 12223920 intron variant T/C snv 0.50 2
rs10994336
ANK3
0.776 0.160 10 60420054 intron variant C/T snv 7.5E-02 2
rs11039149
NR1H3
0.827 0.280 11 47255124 intron variant A/G snv 0.19 2
rs11039409
NUP160
1.000 0.040 11 47814169 intron variant A/C snv 0.22 2
rs11152363
TCF4
1.000 0.040 18 55389957 intron variant G/A snv 0.16 2
rs11209175
GNG12-AS1
1.000 0.040 1 67909145 intron variant C/T snv 0.54 2