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rs1057516832

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(CT;CT) 0 common in clinvar
Make rs1057516832(-;-)
Make rs1057516832(-;CT)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177994159
GenePROP1
is asnp
is mentioned by
dbSNPrs1057516832
dbSNP (old)rs1057516832
ClinGenrs1057516832
ebirs1057516832
HLIrs1057516832
Exacrs1057516832
Gnomadrs1057516832
Varsomers1057516832
Maprs1057516832
PheGenIrs1057516832
Biobankrs1057516832
1000 genomesrs1057516832
hgdprs1057516832
ensemblrs1057516832
gopubmedrs1057516832
geneviewrs1057516832
scholarrs1057516832
googlers1057516832
pharmgkbrs1057516832
gwascentralrs1057516832
openSNPrs1057516832
23andMers1057516832
23andMe allrs1057516832
SNPshotrs1057516832
SNPdbers1057516832
MSV3drs1057516832
GWAS Ctlgrs1057516832
Max Magnitude0
ClinVar
Risk rs1057516832(-;-)
Alt rs1057516832(-;-)
Reference Rs1057516832(CT;CT)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421160_177421161delAG
CLNSRC
CLNACC RCV000411538.1,