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: rs17699658
rs17699658
FOXP1
3 3 71207158 intron variant C/T snv 0.17 0.700 1.000 2 2016 2019
dbSNP: rs17758695
rs17758695
BCL2
10 18 63253621 intron variant C/T snv 2.1E-02 0.700 1.000 2 2016 2019
dbSNP: rs1958078
rs1958078
SMOC1
4 14 69888141 intron variant A/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs2067663
rs2067663
MEF2C ; MEF2C-AS1
3 5 88895818 intron variant C/T snv 0.22 0.700 1.000 2 2016 2019
dbSNP: rs2283847
rs2283847
MN1
7 22 27785411 intron variant C/A;G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs2492301
rs2492301
ZC3H12A ; LINC01137
4 1 37473572 intron variant T/C snv 0.53 0.700 1.000 2 2016 2019
dbSNP: rs2572207
rs2572207
RAB11A ; DENND4A
3 15 65778355 intron variant C/A;T snv 0.700 1.000 2 2016 2017
dbSNP: rs2713936
rs2713936
TEX9
2 15 56253787 intron variant A/C snv 0.32 0.700 1.000 2 2016 2019
dbSNP: rs2836422
rs2836422
ERG
2 21 38466112 intron variant T/A snv 0.46 0.700 1.000 2 2016 2019
dbSNP: rs28601761
rs28601761 		13 1.000 0.040 8 125487789 intron variant C/G snv 0.37 0.700 1.000 2 2016 2019
dbSNP: rs3218097
rs3218097
CCND3
5 6 41937537 intron variant G/A;T snv 0.800 1.000 2 2010 2012
dbSNP: rs35362007
rs35362007
GLRX5 ; SNHG10
3 14 95536861 intron variant G/A snv 0.27 0.700 1.000 2 2016 2019
dbSNP: rs35979828
rs35979828
NFE2
9 12 54292096 intron variant C/T snv 5.0E-02 0.700 1.000 2 2016 2019
dbSNP: rs41444548
rs41444548
TBX21
2 17 47733988 intron variant C/G snv 4.6E-02 4.4E-02 0.700 1.000 2 2016 2019
dbSNP: rs496321
rs496321
LOC101929295
3 11 95153468 intron variant T/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs592423
rs592423 		6 6 139519556 intron variant A/C snv 0.50 0.700 1.000 2 2016 2017
dbSNP: rs61823972
rs61823972
TMCC2
4 1 205232197 intron variant A/C;T snv 0.700 1.000 2 2016 2019
dbSNP: rs62117911
rs62117911
RAB8A
2 19 16131076 intron variant G/A snv 0.14 0.700 1.000 2 2016 2019
dbSNP: rs62160676
rs62160676
MIR4435-2HG
5 2 111410354 intron variant T/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs6494537
rs6494537
RAB11A ; DENND4A
2 15 65759007 intron variant C/G;T snv 0.800 1.000 2 2010 2012
dbSNP: rs68149176
rs68149176
SLC7A5 ; MIR11401
2 16 87852884 intron variant C/G;T snv 0.700 1.000 2 2016 2019
dbSNP: rs6857303
rs6857303
GYPA ; LOC107986317
2 4 144114635 intron variant G/A snv 0.39 0.700 1.000 2 2016 2019
dbSNP: rs7085433
rs7085433
TIMM23
4 1.000 0.040 10 46002468 intron variant C/T snv 9.5E-02 0.700 1.000 2 2010 2017
dbSNP: rs7155454
rs7155454
FNTB ; MAX ; CHURC1-FNTB
4 14 65035521 intron variant G/A snv 0.61 0.700 1.000 2 2012 2017
dbSNP: rs7203560
rs7203560
NPRL3
7 1.000 0.080 16 134391 intron variant T/G snv 2.0E-02 0.800 1.000 2 2013 2017