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rs137853100

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs137853100(A;A)
Make rs137853100(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position177994152
GenePROP1
is asnp
is mentioned by
dbSNPrs137853100
ebirs137853100
HLIrs137853100
Exacrs137853100
Varsomers137853100
Maprs137853100
PheGenIrs137853100
hapmaprs137853100
1000 genomesrs137853100
hgdprs137853100
ensemblrs137853100
gopubmedrs137853100
geneviewrs137853100
scholarrs137853100
googlers137853100
pharmgkbrs137853100
gwascentralrs137853100
openSNPrs137853100
23andMers137853100
23andMe allrs137853100
SNP Nexus

SNPshotrs137853100
SNPdbers137853100
MSV3drs137853100
GWAS Ctlgrs137853100
Max Magnitude0
OMIM601538
Desc
Variant0012
Relatedalso
ClinVar
Risk rs137853100(A;A)
Alt rs137853100(A;A)
Reference rs137853100(G;G)
Significance Pathogenic
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 1
HGVS NC_000005.9:g.177421153C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000008574.6,