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: rs12447690
rs12447690
LOC107984862
3 1.000 0.160 16 88264518 intron variant C/T snv 0.53 0.700 1.000 1 2016 2016
dbSNP: rs12448211
rs12448211 		2 16 88296907 intron variant G/A snv 0.56 0.700 1.000 1 2016 2016
dbSNP: rs1536478
rs1536478
LOC100506532
1 9 134540402 intron variant G/A;C snv 0.700 1.000 1 2016 2016
dbSNP: rs3118515
rs3118515
LOC100506532
2 9 134544468 intron variant G/A;C;T snv 0.700 1.000 1 2016 2016
dbSNP: rs4965359
rs4965359
LRRK1 ; LOC105371026
1 15 101045131 intron variant G/A snv 0.34 0.700 1.000 1 2016 2016
dbSNP: rs10453441
rs10453441
WNT7B
3 1.000 0.040 22 45967859 intron variant A/G snv 0.40 0.700 1.000 2 2016 2018
dbSNP: rs10064391
rs10064391
ADAMTS6
1 5 65390832 intron variant A/G snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs10161679
rs10161679 		1 13 22669506 intergenic variant G/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs10429294
rs10429294
NDUFAF6
1 8 94957094 intron variant C/T snv 0.50 0.700 1.000 1 2018 2018
dbSNP: rs10471310
rs10471310
ADAMTS6
1 5 65253134 intron variant C/T snv 0.37 0.700 1.000 1 2018 2018
dbSNP: rs10980623
rs10980623
LPAR1
1 9 110898257 intron variant A/G snv 0.16 0.700 1.000 1 2018 2018
dbSNP: rs11111869
rs11111869
GLT8D2
1 12 104008707 intron variant G/A snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs11553764
rs11553764
GLT8D2
2 12 104021466 5 prime UTR variant C/T snv 0.13 0.700 1.000 1 2018 2018
dbSNP: rs115781177
rs115781177
LTBP1
1 2 33123427 intron variant A/G snv 5.6E-02 0.700 1.000 1 2018 2018
dbSNP: rs116878472
rs116878472
NT5DC3
1 12 103817214 intron variant T/C snv 1.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs12912010
rs12912010
SMAD3
1 15 67174805 intron variant G/T snv 0.24 0.700 1.000 1 2018 2018
dbSNP: rs13024279
rs13024279 		1 2 234563951 intergenic variant A/G snv 0.47 0.700 1.000 1 2018 2018
dbSNP: rs1309531
rs1309531
CWC27
1 5 65010484 intron variant A/T snv 0.42 0.700 1.000 1 2018 2018
dbSNP: rs13191376
rs13191376
RUNX2 ; RUNX2-AS1
1 6 45554402 intron variant C/G;T snv 0.27 0.700 1.000 1 2018 2018
dbSNP: rs1412710
rs1412710
COL12A1
1 6 75127487 intron variant T/A;C snv 0.700 1.000 1 2018 2018
dbSNP: rs1536482
rs1536482 		3 1.000 0.040 9 134548682 upstream gene variant G/A snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs16920206
rs16920206 		1 10 64725315 intergenic variant T/C snv 2.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs1931656
rs1931656
LINC02542
1 6 81900471 intron variant A/T snv 0.53 0.700 1.000 1 2018 2018
dbSNP: rs2106166
rs2106166 		1 7 93039018 intergenic variant A/T snv 0.44 0.700 1.000 1 2018 2018
dbSNP: rs2419835
rs2419835 		1 10 113536805 intergenic variant C/T snv 0.72 0.700 1.000 1 2018 2018