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rs786204823

From SNPedia

Orientationminus
Geno Mag Summary
(CACCCCATC;CACCCCATC) 0 common in clinvar
Make rs786204823(-;-)
Make rs786204823(-;CACCCCATC)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position49016634
GeneLHB
is asnp
is mentioned by
dbSNPrs786204823
ebirs786204823
HLIrs786204823
Exacrs786204823
Varsomers786204823
Maprs786204823
PheGenIrs786204823
hapmaprs786204823
1000 genomesrs786204823
hgdprs786204823
ensemblrs786204823
gopubmedrs786204823
geneviewrs786204823
scholarrs786204823
googlers786204823
pharmgkbrs786204823
gwascentralrs786204823
openSNPrs786204823
23andMers786204823
23andMe allrs786204823
SNP Nexus

SNPshotrs786204823
SNPdbers786204823
MSV3drs786204823
GWAS Ctlgrs786204823
Max Magnitude0
ClinVar
Risk rs786204823(;)
Alt rs786204823(;)
Reference rs786204823(CACCCCATC;CACCCCATC)
Significance Pathogenic
Disease Isolated lutropin deficiency
Variation info
Gene LHB
CLNDBN Isolated lutropin deficiency
Reversed 1
HGVS NC_000019.9:g.49519891_49519899delGATGGGGTG
CLNSRC OMIM Allelic Variant
CLNACC RCV000169725.4,