Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10256972
C7orf50
7 999367 intron variant A/C snv 0.62 1
rs10445407
SLC38A10
17 81288009 intron variant C/A;T snv 1
rs10934524 3 96431316 intergenic variant C/G;T snv 1
rs10957550
EYA1
8 71382353 intron variant G/A;C snv 1
rs11574358
WRN
8 31147066 missense variant T/G snv 1
rs12143832 1 21378943 regulatory region variant T/C snv 0.44 1
rs1262476
LOC105377992
6 126665850 intron variant A/G;T snv 2
rs12949468
TLK2
17 62516455 non coding transcript exon variant G/A snv 1.0E-02 1
rs13008689
LINC00299
2 8390126 intron variant G/A snv 0.35 1
rs13053175
SSTR3
22 37217269 upstream gene variant C/T snv 0.33 1
rs13118159
UVSSA
4 1371339 intron variant T/C snv 0.55 1
rs1327533
SVEP1
9 110368883 intron variant T/G snv 8.7E-02 1
rs1356888
NRXN1
2 50288880 intron variant T/A;C snv 1
rs138762279 5 174283195 intergenic variant T/- del 0.34 1
rs1416280 6 102438768 intergenic variant C/G snv 0.35 1
rs1425609 3 162964207 intergenic variant G/A snv 0.37 1
rs145672791 21 13377702 intergenic variant G/A snv 8.1E-03 1
rs1487614 4 42267463 non coding transcript exon variant T/C snv 0.65 1
rs16975963
LOC100631378
19 37834896 intron variant C/G snv 0.25 1
rs1950902
MTHFD1
0.776 0.240 14 64415662 missense variant A/G snv 0.83 0.83 11
rs2024714
CDH4
20 61637438 intron variant C/T snv 0.60 1
rs2031577 10 4007811 intergenic variant A/G snv 0.53 1
rs2069837
IL6-AS1 ; IL6
0.724 0.520 7 22728408 intron variant A/C;G snv 18
rs2075650
TOMM40
0.662 0.360 19 44892362 intron variant A/G snv 0.13 0.13 45
rs2149954
LINC02227
0.882 0.080 5 158393594 intron variant C/T snv 0.37 5