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: rs10510097
rs10510097
FGFR2
1 1.000 0.080 10 121568362 intron variant C/T snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs10623258
rs10623258
ADSS1
1 1.000 0.080 14 104745924 non coding transcript exon variant -/TT ins 0.56 0.700 1.000 1 2017 2017
dbSNP: rs10629804
rs10629804
PRDM6
1 1.000 0.080 5 123142307 intron variant -/TTCAC delins 0.72 0.700 1.000 1 2017 2017
dbSNP: rs10644111
rs10644111
AKAP9
1 1.000 0.080 7 92022864 protein altering variant -/AAC delins 0.39 0.46 0.700 1.000 1 2017 2017
dbSNP: rs10760444
rs10760444
LMX1B
1 1.000 0.080 9 126634155 intron variant G/A snv 0.51 0.700 1.000 1 2017 2017
dbSNP: rs10796944
rs10796944
ASH1L
1 1.000 0.080 1 155446537 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10864459
rs10864459
PEX14
1 1.000 0.080 1 10503552 intron variant A/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10871290
rs10871290 		1 1.000 0.080 16 74438798 intron variant C/T snv 0.61 0.700 1.000 1 2009 2009
dbSNP: rs10885405
rs10885405
TCF7L2
1 1.000 0.080 10 113017911 intron variant C/T snv 0.53 0.700 1.000 1 2017 2017
dbSNP: rs10906522
rs10906522
FRMD4A
1 1.000 0.080 10 13865236 intron variant T/A;C snv 0.700 1.000 1 2017 2017
dbSNP: rs10906806
rs10906806
DCLRE1CP1 ; ACBD7-DCLRE1CP1
1 1.000 0.080 10 15029386 upstream gene variant T/C snv 0.41 0.700 1.000 1 2019 2019
dbSNP: rs10923574
rs10923574 		1 1.000 0.080 1 118488075 regulatory region variant A/C;T snv 0.700 1.000 1 2017 2017
dbSNP: rs10995201
rs10995201
ZNF365
1 1.000 0.080 10 62540131 intron variant A/G snv 0.16 0.700 1.000 1 2017 2017
dbSNP: rs11076805
rs11076805
ADCY9
1 1.000 0.080 16 4056787 intron variant C/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11082321
rs11082321
CABLES1
1 1.000 0.080 18 23196687 intron variant G/A snv 0.14 0.700 1.000 1 2014 2014
dbSNP: rs11096688
rs11096688 		1 1.000 0.080 2 20885650 intergenic variant T/C snv 0.86 0.700 1.000 1 2019 2019
dbSNP: rs11117758
rs11117758
ESRRG
1 1.000 0.080 1 217047232 intron variant G/A snv 0.19 0.700 1.000 1 2017 2017
dbSNP: rs111307654
rs111307654
SGCE ; PEG10
1 1.000 0.080 7 94655777 intron variant -/AA;AAA;AAAA delins 0.700 1.000 1 2017 2017
dbSNP: rs111342015
rs111342015
TTBK1
2 1.000 0.080 6 43259403 intron variant G/A;T snv 0.700 1.000 1 2017 2017
dbSNP: rs11146838
rs11146838 		1 1.000 0.080 10 38856846 intergenic variant A/T snv 0.700 1.000 1 2017 2017
dbSNP: rs111549985
rs111549985
ATG10
1 1.000 0.080 5 81972251 5 prime UTR variant C/G snv 0.18 0.700 1.000 1 2017 2017
dbSNP: rs11155804
rs11155804 		1 1.000 0.080 6 151625017 downstream gene variant T/A snv 0.36 0.700 1.000 1 2016 2016
dbSNP: rs111605422
rs111605422
ATE1
1 1.000 0.080 10 121795069 intron variant G/A snv 3.9E-02 0.700 1.000 1 2017 2017
dbSNP: rs111730030
rs111730030
RPL12P42
1 1.000 0.080 19 13158012 intron variant G/T snv 4.7E-02 0.700 1.000 1 2017 2017
dbSNP: rs111780165
rs111780165
TBC1D29P
1 1.000 0.080 17 30560116 splice acceptor variant G/A snv 5.1E-02 5.0E-02 0.700 1.000 1 2017 2017