Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1038822
THADA
1.000 0.120 2 43511034 intron variant T/A;C snv 1
rs1044386
FEM1A
1.000 0.120 19 4795277 3 prime UTR variant G/A snv 0.20 1
rs1045435
PMEL ; RAB5B ; CDK2
1.000 0.120 12 55972376 3 prime UTR variant G/C snv 0.15 1
rs10459247
HSD17B6
1.000 0.120 12 56777732 intron variant T/C snv 0.21 1
rs10495960
GTF2A1L ; STON1-GTF2A1L ; LHCGR
1.000 0.120 2 48732893 missense variant G/A snv 0.18 0.14 1
rs10505648
LINC02055
1.000 0.120 8 136144207 intron variant A/G snv 0.43 1
rs10514258
VCAN-AS1 ; VCAN
1.000 0.120 5 83575938 intron variant A/G snv 0.13 1
rs1056917
RUVBL2 ; LHB
1.000 0.120 19 49016209 synonymous variant A/G snv 0.61 0.65 1
rs1062809
FST
1.000 0.120 5 53484261 missense variant C/A;G snv 1
rs10739076 1.000 0.120 9 5440589 upstream gene variant A/C;T snv 1
rs10760321 1.000 0.120 9 124101917 TF binding site variant A/G snv 0.30 1
rs10865238
FSHR
1.000 0.120 2 49041665 intron variant A/G snv 0.63 1
rs10876920
HSD17B6
1.000 0.120 12 56782391 intron variant C/G;T snv 0.50 1
rs10993397
AOPEP
1.000 0.120 9 94917489 intron variant C/T snv 0.33 1
rs11031010
LOC105376607
1.000 0.120 11 30218631 intron variant C/A snv 0.11 1
rs11171718
SUOX ; RAB5B
1.000 0.120 12 55995838 3 prime UTR variant G/A snv 4.0E-02 1
rs11225154
YAP1
1.000 0.120 11 102172509 intron variant G/A;C snv 1
rs11225161
YAP1
1.000 0.120 11 102199763 intron variant C/T snv 7.0E-02 1
rs1127760
FST
1.000 0.120 5 53484287 missense variant T/A snv 1
rs1127761
FST
1.000 0.120 5 53484289 stop gained T/A;C snv 2.8E-05 1
rs11466313
TGFB1 ; B9D2
1.000 0.120 19 41355432 intron variant -/CTC;CTCATGTCCCTGCCCTCCCTCCTC delins 0.70 1
rs1151996
PPARG
1.000 0.120 3 12404308 intron variant C/A snv 0.70 1
rs11550558
SUOX ; RAB5B
1.000 0.120 12 55992292 3 prime UTR variant A/G snv 0.16 1
rs1158932956
CCNB1
1.000 0.120 5 69168280 frameshift variant -/T ins 4.0E-06 7.0E-06 1
rs1159315
GABRB1
1.000 0.120 4 47001059 intron variant T/C snv 0.46 1