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rs769066903

From SNPedia

Orientationplus
Geno Mag Summary
(CAGCAGCAGCAA;CAGCAGCAGCAA) 0 common in clinvar
Make rs769066903(-;-)
Make rs769066903(-;CAGCAGCAGCAA)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position49016691
GeneLHB
is asnp
is mentioned by
dbSNPrs769066903
ebirs769066903
HLIrs769066903
Exacrs769066903
Varsomers769066903
Maprs769066903
PheGenIrs769066903
hapmaprs769066903
1000 genomesrs769066903
hgdprs769066903
ensemblrs769066903
gopubmedrs769066903
geneviewrs769066903
scholarrs769066903
googlers769066903
pharmgkbrs769066903
gwascentralrs769066903
openSNPrs769066903
23andMers769066903
23andMe allrs769066903
SNP Nexus

SNPshotrs769066903
SNPdbers769066903
MSV3drs769066903
GWAS Ctlgrs769066903
Max Magnitude0
ClinVar
Risk rs769066903(;)
Alt rs769066903(;)
Reference rs769066903(CAGCAGCAGCAA;CAGCAGCAGCAA)
Significance Pathogenic
Disease Isolated lutropin deficiency
Variation info
Gene LHB
CLNDBN Isolated lutropin deficiency
Reversed 0
HGVS NC_000019.9:g.49519948_49519959delCAGCAGCAGCAA
CLNSRC OMIM Allelic Variant
CLNACC RCV000169726.4,