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rs1064797071

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Chromosome5
Position177995931
GenePROP1
is asnp
is mentioned by
dbSNPrs1064797071
dbSNP (old)rs1064797071
ClinGenrs1064797071
ebirs1064797071
HLIrs1064797071
Exacrs1064797071
Gnomadrs1064797071
Varsomers1064797071
Maprs1064797071
PheGenIrs1064797071
Biobankrs1064797071
1000 genomesrs1064797071
hgdprs1064797071
ensemblrs1064797071
gopubmedrs1064797071
geneviewrs1064797071
scholarrs1064797071
googlers1064797071
pharmgkbrs1064797071
gwascentralrs1064797071
openSNPrs1064797071
23andMers1064797071
23andMe allrs1064797071
SNPshotrs1064797071
SNPdbers1064797071
MSV3drs1064797071
GWAS Ctlgrs1064797071
Max Magnitude0
ClinVar
Risk rs1064797071(C;C)
Alt rs1064797071(C;C)
Reference Rs1064797071(G;G)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177422932C>G
CLNSRC
CLNACC RCV000487438.1,