Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs9496567
LOC105377911
6 100154877 intergenic variant G/A snv 0.24 2
rs670401
ARHGAP42
11 100701679 intron variant A/G snv 0.76 3
rs633185
ARHGAP42
0.925 0.080 11 100722807 intron variant G/A;C snv 10
rs604723
ARHGAP42
1.000 0.040 11 100739815 intron variant T/C snv 0.78 9
rs2062331
MSRA
8 10122482 intron variant A/G snv 0.51 2
rs11993089
MSRA
8 10152442 intron variant G/T snv 0.45 1
rs35225200 1.000 0.040 4 102225731 intergenic variant A/C snv 5.4E-02 5
rs13107325
SLC39A8
0.776 0.520 4 102267552 missense variant C/A;T snv 4.0E-06; 4.5E-02 34
rs13135092
SLC39A8
4 102276925 intron variant A/G snv 5.1E-02 4
rs34919878
MSRA
8 10241994 intron variant G/A snv 0.29 2
rs7909591
LOC107984265 ; AS3MT ; BORCS7-ASMT
10 102899261 non coding transcript exon variant G/T snv 0.30 2
rs11786677
MSRA
8 10406750 intron variant A/G snv 0.46 2
rs45490496 14 104806341 downstream gene variant A/T snv 0.45 2
rs2575876
ABCA1
9 104903458 intron variant G/A snv 0.24 7
rs4841409
RP1L1
8 10658864 intron variant A/G snv 0.61 3
rs2392929 7 106773623 upstream gene variant T/A;C;G snv 4
rs13225723 7 106776021 splice region variant G/A snv 0.19 2
rs17035646
CASZ1
1 10736490 intron variant G/A;T snv 6
rs35295665
CASZ1
1 10737371 intron variant -/C delins 2
rs34071855
CASZ1
1 10738432 intron variant C/G;T snv 4
rs13276026
PINX1 ; LOC102723313
8 10752445 intron variant G/A snv 0.56 3
rs139077481 11 107579224 intergenic variant T/C snv 3.2E-03 1
rs4551304
PINX1
8 10807559 intron variant A/G snv 0.65 3
rs7814757
PINX1
8 10817678 intron variant T/C;G snv 2
rs7528419
CELSR2
0.851 0.080 1 109274570 3 prime UTR variant A/G snv 0.23 13