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: rs11953630
rs11953630 		6 5 158418394 intergenic variant C/A;T snv 0.700 1.000 6 2011 2018
dbSNP: rs17080102
rs17080102
PLEKHG1
3 6 150683634 5 prime UTR variant G/C snv 8.6E-02 0.700 1.000 6 2013 2019
dbSNP: rs35444
rs35444 		6 12 115114632 intergenic variant A/G snv 0.38 0.700 1.000 6 2011 2019
dbSNP: rs1173771
rs1173771 		9 5 32814922 regulatory region variant A/G snv 0.65 0.700 1.000 5 2011 2018
dbSNP: rs1327235
rs1327235 		7 20 10988382 intron variant A/G snv 0.46 0.700 1.000 5 2011 2018
dbSNP: rs167479
rs167479
RGL3
5 19 11416089 missense variant T/A;C;G snv 0.700 1.000 5 2016 2019
dbSNP: rs751984
rs751984
LRRC10B
4 11 61510774 3 prime UTR variant T/C snv 0.16 0.700 1.000 5 2016 2019
dbSNP: rs11977526
rs11977526
LOC102723446
3 7 45968511 intron variant G/A;T snv 0.700 1.000 4 2016 2017
dbSNP: rs13112725
rs13112725
NPNT
2 4 105990585 intron variant G/C snv 0.70 0.700 1.000 4 2017 2018
dbSNP: rs13209747
rs13209747 		5 6 126794309 intron variant C/G;T snv 0.36 0.700 1.000 4 2013 2018
dbSNP: rs16849225
rs16849225 		5 2 164050310 intron variant C/T snv 0.19 0.700 1.000 4 2011 2018
dbSNP: rs2306363
rs2306363
SIPA1
7 11 65638129 5 prime UTR variant G/T snv 0.15 0.700 1.000 4 2017 2019
dbSNP: rs2643826
rs2643826 		6 3 27521497 upstream gene variant C/T snv 0.56 0.700 1.000 4 2017 2019
dbSNP: rs2898290
rs2898290
LINC00208
2 8 11576400 non coding transcript exon variant T/C snv 0.49 0.700 1.000 4 2016 2018
dbSNP: rs419076
rs419076
MECOM
6 3 169383098 intron variant T/A;C snv 0.700 1.000 4 2011 2018
dbSNP: rs6015450
rs6015450
ZNF831
7 20 59176062 intron variant A/G snv 0.14 0.700 1.000 4 2011 2018
dbSNP: rs932764
rs932764
PLCE1
6 10 94136183 intron variant A/G snv 0.38 0.700 1.000 4 2011 2017
dbSNP: rs10260816
rs10260816
LOC102723446
2 7 45970501 intron variant C/A;G;T snv 0.700 1.000 3 2017 2019
dbSNP: rs10437954
rs10437954
ARHGEF25 ; DTX3
1 12 57610139 upstream gene variant G/A;C snv 0.700 1.000 3 2018 2019
dbSNP: rs10948071
rs10948071
ZNF318
4 6 43312975 intron variant C/T snv 0.46 0.700 1.000 3 2017 2018
dbSNP: rs11222084
rs11222084
ZBTB44-DT
3 11 130403335 non coding transcript exon variant A/T snv 0.30 0.700 1.000 3 2017 2019
dbSNP: rs1126930
rs1126930
PRKAG1 ; DDN-AS1
5 12 49005349 missense variant G/C snv 2.1E-02 2.1E-02 0.700 1.000 3 2016 2019
dbSNP: rs1173766
rs1173766 		5 5 32804422 intergenic variant T/C snv 0.57 0.700 1.000 3 2011 2018
dbSNP: rs139491786
rs139491786
SLC9A3R2
4 16 2036420 missense variant C/T snv 3.4E-03 3.5E-03 0.700 1.000 3 2017 2019
dbSNP: rs1446468
rs1446468 		4 2 164106976 intron variant T/C snv 0.40 0.700 1.000 3 2017 2018