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: rs76371172
rs76371172
OTUD7A ; LOC105370753
4 0.882 0.040 15 31522252 intron variant T/G snv 9.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs77033326
rs77033326
FAM13A
2 1.000 0.040 4 88856467 intron variant G/A snv 1.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs9577511
rs9577511
GRTP1
4 0.882 0.040 13 113337508 intron variant A/G snv 0.15 0.700 1.000 1 2019 2019
dbSNP: rs9972552
rs9972552
PGBD4
2 1.000 0.040 15 34104712 3 prime UTR variant A/C snv 0.99 0.700 1.000 1 2019 2019
dbSNP: rs112504494
rs112504494
KCNMB2 ; KCNMB2-AS1
1 3 178689358 intron variant G/A snv 7.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs112595860
rs112595860
FGD4
1 12 32487657 intron variant C/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11762112
rs11762112 		1 7 27486673 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs150801052
rs150801052
RBFOX2
1 22 35859882 intron variant T/- delins 1.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs16841143
rs16841143
PTH2R
2 2 208384849 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs182087934
rs182087934 		2 2 183742707 intergenic variant G/A snv 0.700 1.000 1 2018 2018
dbSNP: rs384005
rs384005
MEF2C-AS2
2 5 88709286 intron variant T/C snv 0.70 0.700 1.000 1 2018 2018
dbSNP: rs4053798
rs4053798 		1 6 85233471 intergenic variant A/C snv 1.00 0.700 1.000 1 2018 2018
dbSNP: rs4554696
rs4554696
PDE4B
2 1 65942328 intron variant C/T snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs4809706
rs4809706 		1 20 48577181 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs61606793
rs61606793
KCNMB2 ; KCNMB2-AS1
1 3 178690059 intron variant T/G snv 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs62199592
rs62199592 		2 2 183858773 intergenic variant A/G snv 2.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs6475417
rs6475417
SLC24A2
2 9 20212043 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6661750
rs6661750
PDE4B
2 1 66081201 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs6880062
rs6880062 		1 5 153918465 intergenic variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs72940689
rs72940689 		1 1 80963082 intergenic variant G/A snv 7.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs76426299
rs76426299 		1 8 57438152 regulatory region variant G/A snv 3.1E-02 0.700 1.000 1 2018 2018
dbSNP: rs7862648
rs7862648
ADAMTSL1
1 9 18290859 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs79324256
rs79324256
KCNMB2 ; KCNMB2-AS1
1 3 178688376 intron variant T/C snv 7.5E-02 0.700 1.000 1 2018 2018
dbSNP: rs17173608
rs17173608
RARRES2
8 0.807 0.240 7 150339575 intron variant T/G snv 0.11 0.700 1.000 1 2014 2014
dbSNP: rs17387100
rs17387100
PROM1
3 0.925 0.040 4 15993502 intron variant A/G snv 7.5E-02 0.700 1.000 1 2014 2014