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rs587776682

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GTGGAGCACTCGA;GTGGAGCACTCGA) 0 common in clinvar
Make rs587776682(-;-)
Make rs587776682(-;GTGGAGCACTCGA)
ReferenceGRCh38 38.1/142
Chromosome5
Position177994324
GenePROP1
is asnp
is mentioned by
dbSNPrs587776682
ebirs587776682
HLIrs587776682
Exacrs587776682
Varsomers587776682
Maprs587776682
PheGenIrs587776682
hapmaprs587776682
1000 genomesrs587776682
hgdprs587776682
ensemblrs587776682
gopubmedrs587776682
geneviewrs587776682
scholarrs587776682
googlers587776682
pharmgkbrs587776682
gwascentralrs587776682
openSNPrs587776682
23andMers587776682
23andMe allrs587776682
SNP Nexus

SNPshotrs587776682
SNPdbers587776682
MSV3drs587776682
GWAS Ctlgrs587776682
Max Magnitude0
ClinVar
Risk rs587776682(;)
Alt rs587776682(;)
Reference rs587776682(GTGGAGCACTCGA;GTGGAGCACTCGA)
Significance Other
Disease Pituitary hormone deficiency
Variation info
Gene PROP1
CLNDBN Pituitary hormone deficiency, combined 2
Reversed 0
HGVS NC_000005.9:g.177421325_177421337delGTGGAGCACTCGA
CLNSRC OMIM Allelic Variant
CLNACC RCV000008569.3,