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rs1064793140

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome4
Position67753923
GeneGNRHR
is asnp
is mentioned by
dbSNPrs1064793140
dbSNP (old)rs1064793140
ClinGenrs1064793140
ebirs1064793140
HLIrs1064793140
Exacrs1064793140
Gnomadrs1064793140
Varsomers1064793140
Maprs1064793140
PheGenIrs1064793140
Biobankrs1064793140
1000 genomesrs1064793140
hgdprs1064793140
ensemblrs1064793140
gopubmedrs1064793140
geneviewrs1064793140
scholarrs1064793140
googlers1064793140
pharmgkbrs1064793140
gwascentralrs1064793140
openSNPrs1064793140
23andMers1064793140
23andMe allrs1064793140
SNPshotrs1064793140
SNPdbers1064793140
MSV3drs1064793140
GWAS Ctlgrs1064793140
Max Magnitude0
ClinVar
Risk rs1064793140(G;G)
Alt rs1064793140(G;G)
Reference Rs1064793140(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene GNRHR
CLNDBN not provided
Reversed 1
HGVS NC_000004.11:g.68619641T>C
CLNSRC
CLNACC RCV000478033.1,