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: rs10850407
rs10850407 		1 12 114940232 intergenic variant T/G snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs10872673
rs10872673
CCDC170
1 6 151534458 intron variant G/T snv 0.45 0.700 1.000 1 2019 2019
dbSNP: rs10882397
rs10882397
PLCE1
2 10 94132902 intron variant C/A snv 0.52 0.700 1.000 1 2019 2019
dbSNP: rs10942863
rs10942863
LHFPL2
1 5 78550731 intron variant C/G;T snv 0.39 0.700 1.000 1 2019 2019
dbSNP: rs11017236
rs11017236
LINC02646
1 10 130401217 intron variant T/A snv 0.28 0.700 1.000 1 2008 2008
dbSNP: rs11048457
rs11048457
LOC105369705
1 12 26310241 intron variant G/A snv 0.62 0.700 1.000 1 2019 2019
dbSNP: rs11072508
rs11072508 		2 1.000 0.080 15 74770056 regulatory region variant C/T snv 0.43 0.700 1.000 1 2019 2019
dbSNP: rs11111839
rs11111839
TTC41P
1 12 103916945 intron variant C/A snv 7.9E-02 0.700 1.000 1 2008 2008
dbSNP: rs11130381
rs11130381
CHDH
1 3 53815978 3 prime UTR variant C/T snv 0.47 0.700 1.000 1 2019 2019
dbSNP: rs11191580
rs11191580
NT5C2
13 0.827 0.040 10 103146454 intron variant T/C snv 7.9E-02 0.700 1.000 1 2019 2019
dbSNP: rs11229555
rs11229555
GLYAT
7 0.827 0.120 11 58641214 intron variant G/T snv 0.21 0.700 1.000 1 2019 2019
dbSNP: rs11231711
rs11231711
MACROD1
1 11 64161743 intron variant G/A snv 8.1E-02 0.700 1.000 1 2019 2019
dbSNP: rs112684153
rs112684153
MTRF1
1 13 41275595 intergenic variant T/C;G snv 0.700 1.000 1 2019 2019
dbSNP: rs113230003
rs113230003
PGPEP1
2 19 18350146 intron variant G/A snv 0.25 0.700 1.000 1 2019 2019
dbSNP: rs113602013
rs113602013 		1 18 60252477 intergenic variant G/A;C snv 0.700 1.000 1 2019 2019
dbSNP: rs113898337
rs113898337
HS1BP3
1 2 20567381 intron variant C/G snv 4.1E-03 0.700 1.000 1 2019 2019
dbSNP: rs1149643
rs1149643 		1 1 56163763 intron variant A/T snv 0.49 0.700 1.000 1 2019 2019
dbSNP: rs115262049
rs115262049
LOC112268413
1 2 42969554 regulatory region variant A/T snv 5.6E-02 0.700 1.000 1 2019 2019
dbSNP: rs1154988
rs1154988 		7 3 136206349 upstream gene variant T/A snv 0.76 0.700 1.000 1 2019 2019
dbSNP: rs1155311
rs1155311
DLG2
1 11 83778372 intron variant A/T snv 0.66 0.700 1.000 1 2019 2019
dbSNP: rs11556924
rs11556924
ZC3HC1
21 0.752 0.240 7 130023656 missense variant C/A;T snv 4.0E-06; 0.28 0.700 1.000 1 2019 2019
dbSNP: rs11601694
rs11601694
C1QTNF4
1 11 47593023 intron variant C/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs11605518
rs11605518 		1 11 13248667 intergenic variant A/G snv 0.72 0.700 1.000 1 2019 2019
dbSNP: rs11647570
rs11647570
ADCY9
1 16 4087261 intron variant A/G snv 0.20 0.700 1.000 1 2019 2019
dbSNP: rs11688682
rs11688682 		3 1.000 0.080 2 120590036 intergenic variant G/C snv 0.20 0.700 1.000 1 2019 2019