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rs786204822

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786204822(C;C)
Make rs786204822(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome19
Position49016546
GeneLHB
is asnp
is mentioned by
dbSNPrs786204822
ebirs786204822
HLIrs786204822
Exacrs786204822
Varsomers786204822
Maprs786204822
PheGenIrs786204822
hapmaprs786204822
1000 genomesrs786204822
hgdprs786204822
ensemblrs786204822
gopubmedrs786204822
geneviewrs786204822
scholarrs786204822
googlers786204822
pharmgkbrs786204822
gwascentralrs786204822
openSNPrs786204822
23andMers786204822
23andMe allrs786204822
SNP Nexus

SNPshotrs786204822
SNPdbers786204822
MSV3drs786204822
GWAS Ctlgrs786204822
Max Magnitude0
ClinVar
Risk rs786204822(C,T;C,T)
Alt rs786204822(C,T;C,T)
Reference rs786204822(G;G)
Significance Pathogenic
Disease Isolated lutropin deficiency
Variation info
Gene LHB
CLNDBN Isolated lutropin deficiency
Reversed 1
HGVS NC_000019.9:g.49519803C>A; NC_000019.9:g.49519803C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000169727.4, RCV000169724.4,