Gene: GHRLOS ×
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: rs34911341
rs34911341
GHRL ; GHRLOS
5 0.882 0.200 3 10289835 missense variant C/T snv 7.0E-03 7.3E-03 0.710 1.000 1 2002 2002
dbSNP: rs4684677
rs4684677
GHRL ; GHRLOS
13 0.742 0.360 3 10286769 missense variant T/A snv 0.10 6.6E-02 0.710 < 0.001 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 0.050 1.000 5 2005 2019
dbSNP: rs2075356
rs2075356
GHRL ; GHRLOS
5 0.882 0.160 3 10287125 non coding transcript exon variant T/C snv 8.3E-02 0.010 1.000 1 2013 2013
dbSNP: rs26312
rs26312
GHRL ; GHRLOS
2 0.925 0.080 3 10291174 5 prime UTR variant G/A snv 0.16 0.010 1.000 1 2013 2013
dbSNP: rs26802
rs26802
GHRL ; GHRLOS
3 0.925 0.160 3 10290681 intron variant T/G snv 0.31 0.010 1.000 1 2015 2015