Source: ALL
Variant Gene N. diseases v DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs1001745
rs1001745
RHOQ
1 2 46547920 intron variant T/C snv 0.23 0.700 1.000 1 2012 2012
dbSNP: rs10022109
rs10022109
TET2
1 4 105166665 intron variant A/G snv 0.20 0.700 1.000 1 2018 2018
dbSNP: rs10064975
rs10064975
MTX3
1 5 79981392 3 prime UTR variant A/G snv 0.68 0.700 1.000 1 2012 2012
dbSNP: rs10076188
rs10076188
MCTP1 ; SLF1
1 5 94726834 intron variant C/T snv 0.27 0.700 1.000 1 2012 2012
dbSNP: rs1014530
rs1014530
TRAF1
1 9 120922814 intron variant T/C snv 0.51 0.700 1.000 1 2016 2016
dbSNP: rs10243593
rs10243593 		1 7 39932526 intergenic variant G/A snv 0.44 0.700 1.000 1 2016 2016
dbSNP: rs1026619
rs1026619
QRSL1
1 6 106666486 3 prime UTR variant A/G snv 0.34 0.700 1.000 1 2012 2012
dbSNP: rs10404046
rs10404046
EPS15L1
1 19 16366444 intron variant G/C snv 0.63 0.700 1.000 1 2018 2018
dbSNP: rs10408945
rs10408945
EPS15L1
1 19 16466180 intron variant G/T snv 0.14 0.700 1.000 1 2016 2016
dbSNP: rs10424282
rs10424282
VRK3
1 19 49989603 intron variant C/G;T snv 0.38 0.700 1.000 1 2012 2012
dbSNP: rs10425451
rs10425451 		1 19 54441331 upstream gene variant C/T snv 0.39 0.700 1.000 1 2012 2012
dbSNP: rs10483084
rs10483084 		1 21 41975215 intergenic variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10489208
rs10489208
GPR161
1 1 168125471 intron variant C/T snv 0.11 0.700 1.000 1 2012 2012
dbSNP: rs10496125
rs10496125
SPRED2
1 2 65408072 intron variant C/A snv 9.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10554441
rs10554441
ETV1
1 7 13978399 intron variant ACACACAC/-;AC;ACAC;ACACAC;ACACACACAC;ACACACACACAC delins 0.78 0.700 1.000 1 2016 2016
dbSNP: rs10554589
rs10554589
ANKRD11 ; LOC105371414
1 16 89295870 intron variant ATGTG/- delins 0.83 0.700 1.000 1 2016 2016
dbSNP: rs1059307
rs1059307
SNORD50A ; SNHG5 ; SNORD50B ; LOC107986622
1 6 85678170 non coding transcript exon variant G/T snv 0.45 0.700 1.000 1 2012 2012
dbSNP: rs1060379
rs1060379
ZNF117 ; ERV3-1-ZNF117
1 7 64975111 3 prime UTR variant A/T snv 0.50 0.700 1.000 1 2012 2012
dbSNP: rs1062808
rs1062808
CARD8
1 19 48208219 3 prime UTR variant T/C snv 0.31 0.700 1.000 1 2012 2012
dbSNP: rs1065483
rs1065483
NUP88 ; RABEP1
1 17 5381475 synonymous variant G/A snv 0.53 0.51 0.700 1.000 1 2012 2012
dbSNP: rs10748016
rs10748016 		1 12 65138965 downstream gene variant A/T snv 0.57 0.700 1.000 1 2012 2012
dbSNP: rs10768983
rs10768983
HSD17B12
1 11 43818385 intron variant G/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10777181
rs10777181
POC1B
1 12 89514850 intron variant T/A;C snv 0.700 1.000 1 2012 2012
dbSNP: rs10799505
rs10799505 		1 1 224163321 downstream gene variant C/T snv 0.41 0.700 1.000 1 2012 2012
dbSNP: rs10805888
rs10805888
LINC01331
1 5 74489722 intron variant A/G snv 0.36 0.700 1.000 1 2012 2012