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: rs10076782
rs10076782
RNF145
1 5 159177955 intron variant G/A snv 0.41 0.800 1.000 1 2011 2011
dbSNP: rs10220411
rs10220411
ACTN1-AS1
2 14 68985371 intron variant A/G snv 0.29 0.700 1.000 1 2016 2016
dbSNP: rs10274553
rs10274553
CTB-30L5.1
1 7 106716200 intron variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs10512627
rs10512627
KALRN
1 3 124621375 intron variant G/C snv 0.43 0.800 1.000 1 2011 2011
dbSNP: rs1059196
rs1059196
GP1BB ; SEPT5-GP1BB
3 22 19724571 3 prime UTR variant C/T snv 0.42 0.700 1.000 1 2016 2016
dbSNP: rs10605167
rs10605167
ENDOD1
1 11 95095304 intron variant TCC/-;TCCTCC delins 0.700 1.000 1 2016 2016
dbSNP: rs10813766
rs10813766
DOCK8
1 9 331490 intron variant T/G snv 0.64 0.800 1.000 1 2011 2011
dbSNP: rs10821556
rs10821556 		1 9 134077014 upstream gene variant C/A snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs10886430
rs10886430
GRK5
3 10 119250744 intron variant A/G snv 8.8E-02 0.700 1.000 1 2016 2016
dbSNP: rs10900828
rs10900828 		1 5 134500603 upstream gene variant T/A;C;G snv 0.700 1.000 1 2016 2016
dbSNP: rs10940072
rs10940072
MAST4
2 5 66620956 intron variant G/A snv 0.37 0.700 1.000 1 2016 2016
dbSNP: rs10954750
rs10954750
STYXL1
1 7 76035603 intron variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs10990535
rs10990535
SLC35D2
1 9 96328727 intron variant C/T snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs11030122
rs11030122
STIM1
2 11 3865946 intron variant C/G snv 0.27 0.700 1.000 1 2016 2016
dbSNP: rs11043280
rs11043280
WDR66
1 12 121988737 intron variant T/C snv 0.32 0.700 1.000 1 2016 2016
dbSNP: rs11082304
rs11082304
CABLES1
6 18 23141009 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11121012
rs11121012
CAMTA1
2 1 7734229 intron variant A/G snv 0.62 0.700 1.000 1 2016 2016
dbSNP: rs11121529
rs11121529
KIF1B
1 1 10211630 5 prime UTR variant C/G snv 0.20 0.700 1.000 1 2016 2016
dbSNP: rs11123694
rs11123694
GCC2
1 2 108448107 upstream gene variant C/T snv 0.39 0.700 1.000 1 2016 2016
dbSNP: rs111355755
rs111355755 		1 3 171832858 intron variant G/A snv 0.17 0.700 1.000 1 2012 2012
dbSNP: rs111896493
rs111896493
ADGRE5
1 19 14381256 5 prime UTR variant -/AGTG delins 0.700 1.000 1 2016 2016
dbSNP: rs112346425
rs112346425
AP2B1
1 17 35680792 intron variant G/C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs11235688
rs11235688
P2RY2
1 11 73236889 upstream gene variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs112505971
rs112505971
ANKRD26
13 10 27068541 intron variant A/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs11315757
rs11315757
PPP4R1-AS1
1 18 9617722 intron variant AA/-;A;AAA;AAAA delins 0.700 1.000 1 2016 2016