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rs786204663

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786204663(-;-)
Make rs786204663(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position177994138
GenePROP1
is asnp
is mentioned by
dbSNPrs786204663
ebirs786204663
HLIrs786204663
Exacrs786204663
Varsomers786204663
Maprs786204663
PheGenIrs786204663
hapmaprs786204663
1000 genomesrs786204663
hgdprs786204663
ensemblrs786204663
gopubmedrs786204663
geneviewrs786204663
scholarrs786204663
googlers786204663
pharmgkbrs786204663
gwascentralrs786204663
openSNPrs786204663
23andMers786204663
23andMe allrs786204663
SNP Nexus

SNPshotrs786204663
SNPdbers786204663
MSV3drs786204663
GWAS Ctlgrs786204663
Max Magnitude0
ClinVar
Risk rs786204663(;)
Alt rs786204663(;)
Reference rs786204663(C;C)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421139delG
CLNSRC
CLNACC RCV000169459.1,