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: rs4869317
rs4869317
LNPEP
2 1.000 0.040 5 96956300 intron variant T/A snv 0.22 0.010 1.000 1 2019 2019
dbSNP: rs495225
rs495225
GHSR
4 0.882 0.040 3 172448243 synonymous variant G/A;C;T snv 0.66 0.010 1.000 1 2006 2006
dbSNP: rs533123
rs533123
OPRD1
3 0.882 0.160 1 28814643 intron variant G/A;C snv 0.010 1.000 1 2011 2011
dbSNP: rs554073050
rs554073050
CCK
3 0.925 0.040 3 42263460 synonymous variant G/A snv 1.2E-05 7.0E-06 0.010 1.000 1 2006 2006
dbSNP: rs6318
rs6318
HTR2C ; LOC105373313
42 0.623 0.520 X 114731326 missense variant C/G;T snv 0.010 1.000 1 2003 2003
dbSNP: rs6590474
rs6590474
CNTN5
1 1.000 0.040 11 99982441 intron variant A/C snv 0.71 0.010 1.000 1 2009 2009
dbSNP: rs696217
rs696217
GHRL ; GHRLOS
32 0.662 0.640 3 10289773 missense variant G/T snv 8.8E-02 7.1E-02 0.010 1.000 1 2007 2007
dbSNP: rs737582
rs737582
CNTN5
1 1.000 0.040 11 99992669 intron variant G/A snv 0.39 0.010 1.000 1 2009 2009
dbSNP: rs746682028
rs746682028
BDNF ; BDNF-AS
36 0.645 0.480 11 27658414 missense variant C/A;T snv 4.0E-06; 4.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs750136455
rs750136455
POMC
2 0.925 0.120 2 25161569 missense variant C/T snv 2.5E-05 7.0E-06 0.010 1.000 1 1998 1998
dbSNP: rs752298108
rs752298108
GHRL ; GHRLOS
1 1.000 0.040 3 10286806 missense variant C/T snv 4.0E-05 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs7532266
rs7532266 		1 1.000 0.040 1 23225130 regulatory region variant A/C snv 0.66 0.010 1.000 1 2011 2011
dbSNP: rs774996029
rs774996029
NTSR1
1 1.000 0.040 20 62709682 missense variant G/A snv 4.0E-06 1.4E-05 0.010 1.000 1 2012 2012
dbSNP: rs778902328
rs778902328
NPY ; LOC107986777
1 1.000 0.040 7 24291679 missense variant A/G snv 4.0E-06 7.0E-06 0.010 1.000 1 2007 2007
dbSNP: rs7947224
rs7947224
CNTN5
1 1.000 0.040 11 100002678 intron variant T/C snv 0.39 0.010 1.000 1 2009 2009
dbSNP: rs80326661
rs80326661
POMC
2 0.925 0.120 2 25161244 missense variant T/C snv 5.4E-03 5.4E-03 0.010 1.000 1 1998 1998
dbSNP: rs923768
rs923768
CSGALNACT1
1 1.000 0.040 8 19673452 intron variant T/C snv 0.46 0.010 1.000 1 2018 2018
dbSNP: rs9939609
rs9939609
FTO
98 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2012 2012
dbSNP: rs1473473
rs1473473
TPH2
4 0.925 0.080 12 72010598 intron variant C/A;T snv 0.81 0.020 1.000 2 2011 2013
dbSNP: rs5030980
rs5030980
AGRP ; ATP6V0D1 ; LOC101927837
4 0.925 0.120 16 67483042 missense variant C/T snv 3.2E-02 2.9E-02 0.020 1.000 2 2005 2007
dbSNP: rs53576
rs53576
CAV3 ; OXTR
42 0.641 0.320 3 8762685 intron variant A/G;T snv 0.020 1.000 2 2018 2019
dbSNP: rs726281
rs726281
ESR1
1 1.000 0.040 6 151981443 intron variant G/A snv 0.56 0.020 1.000 2 2010 2014
dbSNP: rs2295193
rs2295193
SYNE1
1 1.000 0.040 6 152131959 intron variant G/A;C snv 0.030 0.667 3 2010 2014
dbSNP: rs4680
rs4680
COMT ; MIR4761
249 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 0.060 0.667 6 2001 2017
dbSNP: rs6265
rs6265
BDNF ; BDNF-AS
272 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 0.080 0.875 8 2004 2016