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: rs11935767
rs11935767
H2AZ1-DT
1 4 100093652 intron variant A/G snv 0.24 0.700 1.000 1 2019 2019
dbSNP: rs17882802
rs17882802
CHUK
1 10 100223656 intron variant G/A snv 0.30 0.700 1.000 1 2019 2019
dbSNP: rs112241539
rs112241539
CASTOR3
1 7 100249614 intron variant C/T snv 0.16 0.700 1.000 1 2019 2019
dbSNP: rs395962
rs395962
LIN28B
6 6 104949543 intron variant T/G snv 0.72 0.700 1.000 1 2018 2018
dbSNP: rs314277
rs314277
LIN28B
6 0.925 0.080 6 104959787 intron variant A/C;G;T snv 0.700 1.000 1 2009 2009
dbSNP: rs2679894
rs2679894
TGFBRAP1
2 2 105254322 upstream gene variant A/G snv 0.43 0.700 1.000 1 2018 2018
dbSNP: rs7861820
rs7861820
LINC01505
2 9 106174393 intron variant T/C snv 0.62 0.700 1.000 1 2009 2009
dbSNP: rs10156597
rs10156597
LINC01505
2 9 106179228 intron variant A/T snv 0.36 0.700 1.000 1 2018 2018
dbSNP: rs2519673
rs2519673 		1 7 106354280 intergenic variant G/A;T snv 0.700 1.000 1 2019 2019
dbSNP: rs17153527
rs17153527 		1 7 106855364 intergenic variant T/C snv 9.3E-02 0.800 1.000 1 2009 2009
dbSNP: rs77100210
rs77100210
YBX3 ; LOC112268104
1 12 10723329 upstream gene variant A/C;T snv 3.4E-02 0.700 1.000 1 2019 2019
dbSNP: rs6975557
rs6975557
NRCAM
1 7 108332853 intron variant A/G snv 0.29 0.800 1.000 1 2013 2013
dbSNP: rs13230316
rs13230316
NRCAM
1 7 108351123 intron variant C/G snv 0.29 0.700 1.000 1 2013 2013
dbSNP: rs12211124
rs12211124
SYCP2L
1 6 10886352 intron variant T/C snv 0.31 0.700 1.000 1 2018 2018
dbSNP: rs9358956
rs9358956
SYCP2L
1 6 10887020 5 prime UTR variant G/C;T snv 0.700 1.000 1 2019 2019
dbSNP: rs6899676
rs6899676
SYCP2L
2 6 10895027 intron variant A/G snv 0.21 0.700 1.000 1 2015 2015
dbSNP: rs2153157
rs2153157
SYCP2L
1 6 10897255 intron variant G/A snv 0.55 0.800 1.000 2 2009 2012
dbSNP: rs9393800
rs9393800
SYCP2L ; LOC101928191
3 6 10951504 intron variant A/G snv 0.20 0.700 1.000 1 2015 2015
dbSNP: rs189596789
rs189596789
SMARCA4
1 19 11078944 intron variant G/A snv 1.9E-03 0.700 1.000 1 2013 2013
dbSNP: rs11195485
rs11195485 		1 10 111244059 intergenic variant C/T snv 4.2E-03 0.700 1.000 1 2013 2013
dbSNP: rs12196873
rs12196873
MFSD4B
2 6 111276855 3 prime UTR variant A/C snv 0.10 0.700 1.000 1 2015 2015
dbSNP: rs7852169
rs7852169
PTGR1 ; ZNF483
2 9 111556114 intron variant C/G snv 0.15 0.700 1.000 1 2018 2018
dbSNP: rs7333181
rs7333181 		2 1.000 0.040 13 111568950 intergenic variant G/A snv 0.11 0.800 1.000 1 2009 2009
dbSNP: rs2921759
rs2921759 		1 8 116898565 intergenic variant T/C snv 0.10 0.700 1.000 1 2018 2018
dbSNP: rs10934420
rs10934420
LOC107986022
1 3 117833264 intron variant T/C snv 0.44 0.700 1.000 1 2018 2018