Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10032729
LINC00504
4 14878321 intron variant G/A snv 0.61 1
rs10043077 5 56397112 intergenic variant T/C snv 0.29 1
rs1004467
CYP17A1 ; CYP17A1-AS1
0.790 0.280 10 102834750 non coding transcript exon variant A/G snv 0.15 0.14 13
rs10048404
WDR7
18 56911251 intron variant C/T snv 0.28 1
rs10059921
TMEM161B
5 88218698 intron variant G/T snv 5.6E-02 1
rs10062049 5 62258054 regulatory region variant C/T snv 0.16 2
rs10069690
TERT
0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs10077885 5 115054424 regulatory region variant C/A snv 0.56 2
rs1008058
PRDM6
5 123099932 missense variant G/A;T snv 0.17 0.12 1
rs1009017
RGS6
14 71999568 intron variant T/A;C snv 1
rs10096777
RP1L1
8 10660990 intron variant G/A snv 0.61 2
rs10107145
XKR6
8 10900703 intron variant A/G;T snv 1
rs1011018
HIPK2
7 139763465 intron variant G/A snv 0.30 1
rs1012089 16 74138074 intron variant C/G;T snv 0.40 1
rs10143078
COX16 ; SYNJ2BP-COX16 ; SYNJ2BP
14 70414772 intron variant A/C snv 6.6E-02 2
rs10147464
LOC105370655
14 98122398 intron variant A/G;T snv 1
rs10149871
HHIPL1
14 99645618 intron variant C/T snv 0.36 1
rs1014988
LOC112268218
1 1748780 upstream gene variant G/A;C snv 1
rs10158347 1 232393998 downstream gene variant A/G snv 0.31 1
rs10160382 11 76416170 downstream gene variant T/C snv 0.39 1
rs10166552
KCNE4
2 223171819 intron variant C/A;G;T snv 4.3E-03 2
rs10167839
UBE2E3
2 181018152 intron variant G/A snv 0.39 1
rs1018148
FBN1
15 48610929 intron variant A/G;T snv 1
rs10182056 2 55463087 intergenic variant A/G snv 0.30 1
rs10182307
COL4A4
2 227010644 intron variant G/A snv 0.48 1