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rs104893836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs104893836(A;G)
Make rs104893836(G;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position67754019
GeneGNRHR
is asnp
is mentioned by
dbSNPrs104893836
ebirs104893836
HLIrs104893836
Exacrs104893836
Varsomers104893836
Maprs104893836
PheGenIrs104893836
hapmaprs104893836
1000 genomesrs104893836
hgdprs104893836
ensemblrs104893836
gopubmedrs104893836
geneviewrs104893836
scholarrs104893836
googlers104893836
pharmgkbrs104893836
gwascentralrs104893836
openSNPrs104893836
23andMers104893836
23andMe allrs104893836
SNP Nexus

SNPshotrs104893836
SNPdbers104893836
MSV3drs104893836
GWAS Ctlgrs104893836
GMAF0.002296
Max Magnitude0
OMIM138850
Desc
Variant0001
Relatedalso
ClinVar
Risk rs104893836(G;G)
Alt rs104893836(G;G)
Reference rs104893836(A;A)
Significance Pathogenic
Disease Hypogonadotropic hypogonadism 7 with or without anosmia
Variation info
Gene GNRHR
CLNDBN Hypogonadotropic hypogonadism 7 with or without anosmia
Reversed 1
HGVS NC_000004.11:g.68619737T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000190591.3,