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: rs10739221
rs10739221
LINC01505
5 0.851 0.080 9 106298549 intron variant T/C;G snv 0.700 1.000 1 2015 2015
dbSNP: rs1148732
rs1148732
GPRC5A ; MIR614
3 0.882 0.080 12 12915357 3 prime UTR variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs11532907
rs11532907
MTAP
3 0.882 0.080 9 21844773 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs1484375
rs1484375
LINC01505
3 0.882 0.080 9 106305280 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs2695237
rs2695237 		3 0.882 0.080 1 226415934 upstream gene variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs45575338
rs45575338
TASOR2
3 0.882 0.080 10 5742188 missense variant A/C;G snv 0.19 0.700 1.000 1 2018 2018
dbSNP: rs4731742
rs4731742
LINC-PINT
3 0.882 0.080 7 131070053 intron variant G/A;C snv 0.700 1.000 1 2015 2015
dbSNP: rs4778138
rs4778138
OCA2
6 0.851 0.080 15 28090674 intron variant A/G;T snv 0.700 1.000 1 2015 2015
dbSNP: rs7041168
rs7041168 		3 0.882 0.080 9 107936435 intergenic variant G/A;T snv 0.700 1.000 1 2015 2015
dbSNP: rs869329
rs869329
MTAP
4 0.851 0.080 9 21804694 intron variant A/G;T snv 0.700 1.000 1 2018 2018
dbSNP: rs186133190
rs186133190
WDPCP
3 0.882 0.080 2 63550724 intron variant T/C snv 4.9E-04 0.700 1.000 1 2015 2015
dbSNP: rs117648907
rs117648907
FMN1
3 0.882 0.080 15 32985509 intron variant C/T snv 1.4E-02 0.700 1.000 1 2018 2018
dbSNP: rs184628474
rs184628474
TTC7B
3 0.882 0.080 14 90719521 intron variant G/A snv 2.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs56238684
rs56238684
PIGU
4 0.882 0.080 20 34648892 intron variant G/C snv 4.2E-02 0.700 1.000 1 2018 2018
dbSNP: rs2290419
rs2290419
LOC338694
3 0.882 0.080 11 69152181 intron variant A/G snv 4.6E-02 0.700 1.000 1 2015 2015
dbSNP: rs75570604
rs75570604
FANCA
4 0.851 0.080 16 89780269 intron variant G/C snv 4.7E-02 0.700 1.000 1 2018 2018
dbSNP: rs55875066
rs55875066
HDAC4
3 0.882 0.080 2 239154306 intron variant C/T snv 6.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs75691080
rs75691080 		3 0.882 0.080 20 63638397 downstream gene variant C/T snv 9.1E-02 0.700 1.000 1 2015 2015
dbSNP: rs73008229
rs73008229
ATM ; C11orf65
3 0.882 0.080 11 108316962 intron variant G/A snv 0.11 0.700 1.000 1 2018 2018
dbSNP: rs12596638
rs12596638
FTO
3 0.882 0.080 16 54081917 intron variant G/A snv 0.18 0.700 1.000 1 2018 2018
dbSNP: rs10830253
rs10830253
TYR
4 0.851 0.080 11 89294875 intron variant T/G snv 0.29 0.700 1.000 1 2018 2018
dbSNP: rs1636744
rs1636744
AHR
4 0.851 0.080 7 16944656 intron variant C/T snv 0.31 0.700 1.000 2 2015 2018
dbSNP: rs10816595
rs10816595 		4 0.851 0.080 9 107947454 regulatory region variant A/G snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs72704658
rs72704658
ARNT
3 0.882 0.080 1 150860534 intron variant T/C snv 0.33 0.700 1.000 1 2018 2018
dbSNP: rs251464
rs251464
PPARGC1B
5 0.851 0.080 5 149816671 intron variant G/C snv 0.36 0.700 1.000 1 2018 2018