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rs1057517027

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(AC;AC) 0 common in clinvar
Make rs1057517027(-;-)
Make rs1057517027(-;AC)
ReferenceGRCh38.p7 38.3/150
Chromosome5
Position177992999
GenePROP1
is asnp
is mentioned by
dbSNPrs1057517027
dbSNP (old)rs1057517027
ClinGenrs1057517027
ebirs1057517027
HLIrs1057517027
Exacrs1057517027
Gnomadrs1057517027
Varsomers1057517027
Maprs1057517027
PheGenIrs1057517027
Biobankrs1057517027
1000 genomesrs1057517027
hgdprs1057517027
ensemblrs1057517027
gopubmedrs1057517027
geneviewrs1057517027
scholarrs1057517027
googlers1057517027
pharmgkbrs1057517027
gwascentralrs1057517027
openSNPrs1057517027
23andMers1057517027
23andMe allrs1057517027
SNPshotrs1057517027
SNPdbers1057517027
MSV3drs1057517027
GWAS Ctlgrs1057517027
Max Magnitude0
ClinVar
Risk rs1057517027(-;-)
Alt rs1057517027(-;-)
Reference Rs1057517027(AC;AC)
Significance Probable-Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177420000_177420001delGT
CLNSRC
CLNACC RCV000409831.1,