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: rs12429545
rs12429545 		4 13 53528071 intron variant G/A;T snv 0.12 0.700 1.000 10 2015 2019
dbSNP: rs3810291
rs3810291
ZC3H4
9 19 47065746 3 prime UTR variant G/A snv 0.50 0.700 1.000 10 2010 2019
dbSNP: rs13021737
rs13021737 		2 2 632348 intergenic variant A/G snv 0.85 0.700 1.000 8 2015 2019
dbSNP: rs10132280
rs10132280 		6 14 25458973 intergenic variant C/A snv 0.37 0.700 1.000 7 2015 2019
dbSNP: rs17024393
rs17024393
GNAT2
4 1 109612066 intron variant T/C snv 4.6E-02 0.700 1.000 7 2015 2019
dbSNP: rs17405819
rs17405819 		3 8 75894349 intergenic variant T/C snv 0.24 0.700 1.000 7 2015 2019
dbSNP: rs1928295
rs1928295 		3 9 117616205 intergenic variant T/C snv 0.45 0.700 1.000 7 2015 2019
dbSNP: rs2365389
rs2365389
FHIT
3 3 61250788 intron variant C/T snv 0.56 0.700 1.000 7 2015 2018
dbSNP: rs6864049
rs6864049
LINC02240 ; LOC105379158
2 5 124994829 intron variant A/C;G;T snv 0.700 1.000 7 2015 2019
dbSNP: rs11165643
rs11165643 		2 1 96458541 intergenic variant C/T snv 0.48 0.700 1.000 6 2015 2019
dbSNP: rs1167827
rs1167827
HIP1
5 7 75533848 3 prime UTR variant G/A snv 0.37 0.700 1.000 6 2015 2018
dbSNP: rs12885454
rs12885454
LOC102724934
4 14 29267632 non coding transcript exon variant C/A snv 0.27 0.700 1.000 6 2015 2019
dbSNP: rs13191362
rs13191362
PRKN
3 6 162612318 intron variant A/G snv 8.7E-02 0.700 1.000 6 2015 2019
dbSNP: rs16907751
rs16907751 		1 8 80463222 intron variant C/T snv 0.10 0.700 1.000 6 2015 2019
dbSNP: rs2033529
rs2033529
TDRG1
4 6 40380914 intron variant A/C;G snv 0.700 1.000 6 2015 2019
dbSNP: rs2228213
rs2228213
HIVEP1
1 6 12124622 missense variant G/A snv 0.30 0.26 0.700 1.000 6 2015 2019
dbSNP: rs7124681
rs7124681
CELF1
2 11 47508395 intron variant C/A snv 0.36 0.700 1.000 6 2015 2019
dbSNP: rs7599312
rs7599312
LOC107985979
3 2 212548507 regulatory region variant G/A snv 0.29 0.700 1.000 6 2015 2019
dbSNP: rs10920678
rs10920678
BRINP3
1 1 190270777 intron variant A/G snv 0.58 0.700 1.000 5 2015 2019
dbSNP: rs17724992
rs17724992
PGPEP1
1 19 18344015 intron variant A/G snv 0.23 0.700 1.000 5 2015 2018
dbSNP: rs205262
rs205262
ILRUN
2 6 34595387 intron variant A/G snv 0.38 0.700 1.000 5 2015 2018
dbSNP: rs2245368
rs2245368
DTX2P1-UPK3BP1-PMS2P11 ; LOC105375361
3 7 76978826 non coding transcript exon variant C/T snv 0.80 0.700 1.000 5 2015 2018
dbSNP: rs2650492
rs2650492
SBK1
5 16 28322090 3 prime UTR variant G/A snv 0.20 0.700 1.000 5 2015 2018
dbSNP: rs3888190
rs3888190
ATP2A1
3 16 28878165 upstream gene variant C/A;T snv 0.35 0.700 1.000 5 2015 2017
dbSNP: rs4740619
rs4740619
CCDC171
1 9 15634328 intron variant T/A;C snv 0.700 1.000 5 2015 2019