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: rs11165623
rs11165623 		2 1 96427444 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs12086130
rs12086130
FAF1
1 1 50707931 intron variant C/T snv 0.12 0.700 1.000 1 2015 2015
dbSNP: rs17024393
rs17024393
GNAT2
4 1 109612066 intron variant T/C snv 4.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs17391694
rs17391694 		6 0.882 0.120 1 78157942 regulatory region variant C/T snv 7.8E-02 0.700 1.000 1 2015 2015
dbSNP: rs2605098
rs2605098
LYPLAL1-AS1 ; LOC107985272
1 1 219470307 intergenic variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs2801966
rs2801966 		1 1 41410365 intergenic variant T/A snv 0.95 0.700 1.000 1 2017 2017
dbSNP: rs2820443
rs2820443 		8 0.882 0.120 1 219580167 regulatory region variant T/C snv 0.23 0.700 1.000 1 2015 2015
dbSNP: rs532504
rs532504 		2 1 177909798 intron variant G/A snv 0.17 0.700 1.000 1 2017 2017
dbSNP: rs543874
rs543874 		11 1.000 0.080 1 177920345 upstream gene variant A/G snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs6604866
rs6604866
TNNI3K ; FPGT-TNNI3K ; LRRC53
1 1 74526862 intron variant G/C snv 0.44 0.700 1.000 1 2015 2015
dbSNP: rs6678622
rs6678622
ZZZ3
1 1 77626794 intron variant C/T snv 0.29 0.700 1.000 1 2015 2015
dbSNP: rs6685593
rs6685593 		1 1 203546947 regulatory region variant T/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs7531118
rs7531118
LOC105378797
7 1.000 0.080 1 72371556 intron variant T/C snv 0.40 0.700 1.000 1 2015 2015
dbSNP: rs10200566
rs10200566
ADCY3
1 2 24907593 intron variant T/G snv 0.54 0.700 1.000 1 2019 2019
dbSNP: rs10929925
rs10929925 		3 2 6015425 intergenic variant C/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs11676272
rs11676272
ADCY3
5 1.000 0.040 2 24918669 missense variant A/G snv 0.47 0.57 0.700 1.000 1 2015 2015
dbSNP: rs1320330
rs1320330 		2 2 622225 intergenic variant T/A;G snv 0.700 1.000 1 2017 2017
dbSNP: rs1561277
rs1561277
ZRANB3
1 2 135334491 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs355838
rs355838
COBLL1
1 2 164762653 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs4988235
rs4988235
MCM6
19 0.752 0.400 2 135851076 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs62104180
rs62104180 		4 2 466003 intergenic variant G/A snv 2.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs6751993
rs6751993 		2 2 635864 intergenic variant A/G snv 0.85 0.700 1.000 1 2019 2019
dbSNP: rs6755502
rs6755502 		3 2 635721 intergenic variant T/C snv 0.85 0.700 1.000 1 2015 2015
dbSNP: rs887912
rs887912 		6 1.000 0.080 2 59075742 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs13098327
rs13098327
CADM2
2 3 85771031 intron variant G/A snv 0.15 0.700 1.000 1 2015 2015