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: rs2069837
rs2069837
IL6 ; IL6-AS1
18 0.724 0.520 7 22728408 intron variant A/C;G snv 0.700 1.000 2 2016 2019
dbSNP: rs10445407
rs10445407
SLC38A10
1 17 81288009 intron variant C/A;T snv 0.800 1.000 1 2010 2010
dbSNP: rs10934524
rs10934524 		1 3 96431316 intergenic variant C/G;T snv 0.700 1.000 1 2016 2016
dbSNP: rs10957550
rs10957550
EYA1
1 8 71382353 intron variant G/A;C snv 0.700 1.000 1 2014 2014
dbSNP: rs11574358
rs11574358
WRN
1 8 31147066 missense variant T/G snv 0.700 1.000 1 2015 2015
dbSNP: rs1262476
rs1262476
LOC105377992
2 6 126665850 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs1356888
rs1356888
NRXN1
1 2 50288880 intron variant T/A;C snv 0.800 1.000 1 2010 2010
dbSNP: rs2229188
rs2229188
CYP51A1 ; CYP51A1-AS1
1 7 92134309 missense variant A/G snv 4.3E-06 0.700 1.000 1 2015 2015
dbSNP: rs2292664
rs2292664
RIMBP2
1 12 130437119 missense variant G/A;C snv 9.2E-06; 5.3E-04 0.700 1.000 1 2015 2015
dbSNP: rs2440012
rs2440012
ANKRD20A9P
1 13 18865983 intron variant C/A;G snv 0.700 1.000 1 2016 2016
dbSNP: rs2882281
rs2882281 		1 13 89970201 intergenic variant C/A;G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs4904670
rs4904670
NRDE2
1 14 90303866 intron variant C/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs62127362
rs62127362
CEP89
1 19 32967573 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs6813479
rs6813479 		1 4 136739228 intergenic variant T/A;C snv 0.800 1.000 1 2010 2010
dbSNP: rs6915183
rs6915183 		1 6 166292681 intergenic variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs7039467
rs7039467
CDKN2B-AS1
1 9 22056214 intron variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs7894051
rs7894051
ECHS1
1 10 133370917 intron variant C/A;G snv 0.700 1.000 1 2015 2015
dbSNP: rs9616906
rs9616906 		1 22 50666252 upstream gene variant G/A;C snv 0.800 1.000 1 2010 2010
dbSNP: rs9876781
rs9876781
CCDC51 ; ATRIP ; ATRIP-TREX1
1 3 48445934 intron variant A/G;T snv 0.800 1.000 1 2010 2010
dbSNP: rs145672791
rs145672791 		1 21 13377702 intergenic variant G/A snv 8.1E-03 0.700 1.000 1 2016 2016
dbSNP: rs12949468
rs12949468
TLK2
1 17 62516455 non coding transcript exon variant G/A snv 1.0E-02 0.700 1.000 1 2015 2015
dbSNP: rs4639950
rs4639950
MFRP ; C1QTNF5
1 11 119345845 missense variant T/C snv 4.0E-03 1.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs7676745
rs7676745
GPR78
1 4 8563820 intron variant G/A snv 5.3E-02 0.700 1.000 1 2019 2019
dbSNP: rs7412
rs7412
APOE
47 0.641 0.640 19 44908822 missense variant C/T snv 6.2E-02 7.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs1327533
rs1327533
SVEP1
1 9 110368883 intron variant T/G snv 8.7E-02 0.800 1.000 1 2010 2010