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rs766673446

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs766673446(C;C)
Make rs766673446(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome5
Position177994114
GenePROP1
is asnp
is mentioned by
dbSNPrs766673446
ebirs766673446
HLIrs766673446
Exacrs766673446
Varsomers766673446
Maprs766673446
PheGenIrs766673446
hapmaprs766673446
1000 genomesrs766673446
hgdprs766673446
ensemblrs766673446
gopubmedrs766673446
geneviewrs766673446
scholarrs766673446
googlers766673446
pharmgkbrs766673446
gwascentralrs766673446
openSNPrs766673446
23andMers766673446
23andMe allrs766673446
SNP Nexus

SNPshotrs766673446
SNPdbers766673446
MSV3drs766673446
GWAS Ctlgrs766673446
Max Magnitude0
ClinVar
Risk rs766673446(A,C;A,C)
Alt rs766673446(A,C;A,C)
Reference rs766673446(G;G)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 0
HGVS NC_000005.9:g.177421115G>A
CLNSRC
CLNACC RCV000169361.1,