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: rs10786714
rs10786714
CYP17A1 ; LOC107984264
2 10 102838849 intron variant G/C snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs114811870
rs114811870
HLA-B ; MIR6891
1 6 31357161 5 prime UTR variant C/T snv 4.2E-02 8.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs115310850
rs115310850 		1 6 31855479 downstream gene variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs115448006
rs115448006
MDC1 ; MDC1-AS1
1 6 30701491 intron variant G/T snv 1.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs11575837
rs11575837
NCR3
2 1.000 0.200 6 31592893 5 prime UTR variant C/T snv 2.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs140054334
rs140054334
PRRC2A
1 6 31619265 upstream gene variant C/T snv 4.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs145214406
rs145214406 		1 6 31072878 regulatory region variant -/AA;AAA delins 0.700 1.000 1 2019 2019
dbSNP: rs145827824
rs145827824 		1 6 32135972 intergenic variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs148331983
rs148331983 		1 6 32514378 downstream gene variant -/TGTTTATCCATTT delins 0.700 1.000 1 2019 2019
dbSNP: rs151302046
rs151302046
LINC00243
1 6 30807354 intron variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs1802127
rs1802127
MSH5 ; SAPCD1 ; MSH5-SAPCD1
1 6 31762148 missense variant C/T snv 3.0E-02 5.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs200025476
rs200025476 		1 6 32715787 upstream gene variant A/T snv 5.5E-02 0.700 1.000 1 2019 2019
dbSNP: rs6912701
rs6912701 		1 6 32415796 TF binding site variant C/T snv 6.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs6935999
rs6935999 		1 6 32424980 intergenic variant G/A snv 4.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs6937167
rs6937167 		1 6 32450017 downstream gene variant A/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs73729220
rs73729220
TSBP1-AS1
1 6 32374342 intron variant A/G snv 3.8E-02 0.700 1.000 1 2019 2019
dbSNP: rs7759215
rs7759215 		1 6 31435848 intron variant C/G;T snv 0.700 1.000 1 2019 2019
dbSNP: rs79040733
rs79040733 		1 6 32505230 intergenic variant T/G snv 0.700 1.000 1 2019 2019
dbSNP: rs9268559
rs9268559 		1 6 32421614 intergenic variant A/G snv 4.9E-02 0.700 1.000 1 2019 2019