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: rs10195252
rs10195252
COBLL1
7 0.925 0.080 2 164656581 intron variant T/C snv 0.48 0.800 1.000 1 2010 2010
dbSNP: rs10892151
rs10892151
DSCAML1 ; LOC105369515
3 1.000 11 117661016 intron variant C/T snv 9.7E-02 0.800 1.000 1 2008 2008
dbSNP: rs1121980
rs1121980
FTO
18 0.807 0.240 16 53775335 intron variant G/A;C snv 0.800 1.000 1 2013 2013
dbSNP: rs11823543
rs11823543
ZPR1
3 11 116778419 3 prime UTR variant G/A snv 0.11 0.800 1.000 1 2011 2011
dbSNP: rs11825181
rs11825181
BUD13
2 11 116755542 intron variant G/A snv 0.10 0.800 1.000 1 2011 2011
dbSNP: rs13022873
rs13022873
ZNF512
7 0.882 0.120 2 27592643 intron variant A/C;T snv 0.800 1.000 1 2011 2011
dbSNP: rs2954026
rs2954026 		2 8 125472284 intron variant T/G snv 0.76 0.800 1.000 1 2011 2011
dbSNP: rs3749147
rs3749147
GPN1 ; CCDC121
8 0.882 0.120 2 27629051 missense variant G/A snv 0.23 0.20 0.800 1.000 1 2011 2011
dbSNP: rs7679
rs7679
PCIF1
9 0.925 0.160 20 45947863 3 prime UTR variant T/C snv 0.13 0.800 1.000 1 2009 2009
dbSNP: rs7819412
rs7819412
XKR6
6 0.827 0.120 8 11187652 intron variant G/A;T snv 0.800 1.000 1 2009 2009
dbSNP: rs8077889
rs8077889
MPP3
1 17 43800798 downstream gene variant A/C snv 0.19 0.800 1.000 1 2013 2013
dbSNP: rs1000879
rs1000879
VIL1
3 2 218439407 intron variant G/A snv 4.1E-02 0.700 1.000 1 2012 2012
dbSNP: rs1002487
rs1002487
RPS6KA1
1 1 26539480 intron variant T/C snv 5.3E-02 0.700 1.000 1 2018 2018
dbSNP: rs10033119
rs10033119
NPY1R
1 4 163324702 3 prime UTR variant A/G snv 7.9E-02 0.700 1.000 1 2018 2018
dbSNP: rs10047459
rs10047459
SIK3 ; APOA1-AS
1 11 116851110 intron variant C/T snv 0.80 0.700 1.000 1 2012 2012
dbSNP: rs10047462
rs10047462
SIK3 ; APOA1-AS
3 11 116851325 intron variant G/C;T snv 0.700 1.000 1 2012 2012
dbSNP: rs10054063
rs10054063 		4 5 173965395 downstream gene variant A/T snv 0.26 0.700 1.000 1 2018 2018
dbSNP: rs10055011
rs10055011
CERT1
1 5 75502331 intron variant G/A snv 0.12 0.700 1.000 1 2009 2009
dbSNP: rs1009360
rs1009360
LINC02245 ; LINC02576 ; LOC107984063
2 2 65048915 intron variant T/C snv 0.51 0.700 1.000 1 2018 2018
dbSNP: rs10101067
rs10101067
EYA1
2 8 71495139 intron variant G/C snv 6.2E-02 0.700 1.000 1 2019 2019
dbSNP: rs1011731
rs1011731
PIGC ; DNM3
4 1 172377408 intron variant G/A snv 0.46 0.700 1.000 1 2017 2017
dbSNP: rs10118611
rs10118611
BNC2
1 9 16597467 intron variant G/A snv 3.0E-02 0.700 1.000 1 2012 2012
dbSNP: rs10119
rs10119
TOMM40
5 0.925 0.080 19 44903416 3 prime UTR variant G/A snv 0.28 0.700 1.000 1 2012 2012
dbSNP: rs10120653
rs10120653
RXRA
3 9 134415237 intron variant G/T snv 1.2E-02 0.700 1.000 1 2012 2012
dbSNP: rs10125024
rs10125024
RXRA
1 9 134407131 intron variant C/T snv 1.5E-02 0.700 1.000 1 2012 2012