Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10876550
COPZ1
12 54318524 intron variant G/A snv 0.68 2
rs10893909
SENCR ; FLI1
11 128695139 intron variant C/T snv 0.18 1
rs10914144
DNM3
1 171980610 intron variant T/C snv 0.78 3
rs10919585
MIR181A1HG
1 198806192 intron variant T/C snv 0.52 1
rs10940072
MAST4
5 66620956 intron variant G/A snv 0.37 2
rs10974808
RCL1
9 4840380 intron variant A/G snv 9.0E-02 3
rs10984466
HEMGN
9 97945710 upstream gene variant A/G snv 0.31 1
rs11066301
PTPN11
0.827 0.200 12 112433568 intron variant A/G snv 0.30 12
rs11071720
TPM1-AS ; TPM1
15 63049797 intron variant T/C;G snv 3
rs11082304
CABLES1
18 23141009 intron variant G/C;T snv 6
rs11083766
BLOC1S3 ; EXOC3L2 ; MARK4
19 45212232 intron variant T/C snv 0.26 2
rs11121845
PLOD1
1 11968598 intron variant C/T snv 0.50 1
rs111350029
PIEZO1 ; LOC100289580
16 88730362 intron variant -/AGGCGG delins 1
rs11142444
LOC101927086
9 70451220 intergenic variant C/G;T snv 1
rs11175492
RASSF3
12 64641442 intron variant A/G snv 0.19 1
rs111941366
RHCE
1 25409878 intron variant C/T snv 0.30 2
rs11217191
CBL
11 119223937 intron variant G/A;T snv 1
rs11240408 1 205295408 intergenic variant A/C;G;T snv 1
rs112505971
ANKRD26
10 27068541 intron variant A/C;G snv 13
rs112790992
BRF1
14 105291880 intron variant A/C snv 0.31 1
rs11294619
PAK2
3 196784238 intron variant A/- delins 1
rs113128512
PDGFC
4 156761036 3 prime UTR variant T/C snv 6.7E-02 1
rs113373353
RASSF3
12 64613902 intron variant C/T snv 6.9E-02 1
rs11348701
ATXN2
12 111452430 3 prime UTR variant TTTT/-;T;TT;TTT;TTTTT;TTTTTT delins 0.31 1
rs11382616
RCOR1
14 102615129 intron variant C/-;CC;CCC;CCCC;CCCCC delins 1