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: rs11076008
rs11076008
FTO
2 0.925 0.120 16 53893411 intron variant G/A;C snv 0.010 1.000 1 2014 2014
dbSNP: rs1293713
rs1293713
LOC105372577
1 1.000 0.080 20 24301594 intron variant G/T snv 0.43 0.010 1.000 1 2013 2013
dbSNP: rs244123
rs244123
PKIG
1 1.000 0.080 20 44560637 intron variant T/C snv 0.24 0.010 1.000 1 2013 2013
dbSNP: rs587777178
rs587777178
LZTR1
3 0.925 0.080 22 20995865 missense variant C/T snv 4.4E-05 6.3E-05 0.010 1.000 1 2019 2019
dbSNP: rs770992098
rs770992098
NEB
2 1.000 0.080 2 151724954 missense variant T/C snv 8.0E-06 7.0E-06 0.010 1.000 1 2019 2019
dbSNP: rs886041033
rs886041033
POFUT1
2 0.925 0.080 20 32216660 frameshift variant A/- delins 0.010 1.000 1 2013 2013
dbSNP: rs998259
rs998259
GCH1
3 1.000 0.080 14 54888313 intron variant C/A;T snv 0.010 1.000 1 2010 2010