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rs1057516846

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057516846(A;G)
Make rs1057516846(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177994340
GenePROP1
is asnp
is mentioned by
dbSNPrs1057516846
dbSNP (old)rs1057516846
ClinGenrs1057516846
ebirs1057516846
HLIrs1057516846
Exacrs1057516846
Gnomadrs1057516846
Varsomers1057516846
Maprs1057516846
PheGenIrs1057516846
Biobankrs1057516846
1000 genomesrs1057516846
hgdprs1057516846
ensemblrs1057516846
gopubmedrs1057516846
geneviewrs1057516846
scholarrs1057516846
googlers1057516846
pharmgkbrs1057516846
gwascentralrs1057516846
openSNPrs1057516846
23andMers1057516846
23andMe allrs1057516846
SNPshotrs1057516846
SNPdbers1057516846
MSV3drs1057516846
GWAS Ctlgrs1057516846
Max Magnitude0
ClinVar
Risk rs1057516846(G;G)
Alt rs1057516846(G;G)
Reference Rs1057516846(A;A)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421341T>C
CLNSRC
CLNACC RCV000410070.1,