Source: BEFREE ×
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: rs1051168
rs1051168
NMB
2 1.000 0.080 15 84657289 missense variant G/C;T snv 4.5E-06; 0.22 0.010 1.000 1 2011 2011
dbSNP: rs1137101
rs1137101
LEPR
77 0.554 0.760 1 65592830 missense variant A/G snv 0.51 0.50 0.010 1.000 1 2009 2009
dbSNP: rs1258628899
rs1258628899
PYY
1 17 43953174 synonymous variant G/A snv 7.0E-06 0.010 1.000 1 2008 2008
dbSNP: rs17782313
rs17782313 		26 0.683 0.480 18 60183864 intergenic variant T/C snv 0.24 0.010 1.000 1 2014 2014
dbSNP: rs2878329
rs2878329
OR7D4
1 19 9215066 intron variant C/T snv 0.14 0.010 1.000 1 2012 2012
dbSNP: rs5443
rs5443
GNB3 ; CDCA3
106 0.532 0.760 12 6845711 synonymous variant C/T snv 0.36 0.44 0.010 1.000 1 2009 2009
dbSNP: rs5574
rs5574
NPY ; LOC107986777
5 0.882 0.200 7 24289514 synonymous variant C/T snv 0.43 0.43 0.010 1.000 1 2008 2008
dbSNP: rs572169
rs572169
GHSR
4 0.882 0.160 3 172447937 synonymous variant C/T snv 0.31 0.24 0.010 1.000 1 2008 2008
dbSNP: rs781443388
rs781443388
NPY2R
1 4 155214416 synonymous variant G/A snv 1.6E-05 2.1E-05 0.010 1.000 1 2008 2008
dbSNP: rs992472
rs992472
DNMT3B
1 20 32797463 intron variant G/T snv 0.49 0.010 1.000 1 2009 2009
dbSNP: rs992990
rs992990
GAD2
1 10 26278252 intron variant C/A;G snv 0.37 0.010 1.000 1 2009 2009
dbSNP: rs9939609
rs9939609
FTO
80 0.559 0.720 16 53786615 intron variant T/A snv 0.41 0.010 1.000 1 2009 2009