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rs104893837

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893837(A;A)
Make rs104893837(A;G)
ReferenceGRCh38 38.1/142
Chromosome4
Position67740682
GeneGNRHR
is asnp
is mentioned by
dbSNPrs104893837
ebirs104893837
HLIrs104893837
Exacrs104893837
Varsomers104893837
Maprs104893837
PheGenIrs104893837
hapmaprs104893837
1000 genomesrs104893837
hgdprs104893837
ensemblrs104893837
gopubmedrs104893837
geneviewrs104893837
scholarrs104893837
googlers104893837
pharmgkbrs104893837
gwascentralrs104893837
openSNPrs104893837
23andMers104893837
23andMe allrs104893837
SNP Nexus

SNPshotrs104893837
SNPdbers104893837
MSV3drs104893837
GWAS Ctlgrs104893837
GMAF0.0009183
Max Magnitude0
OMIM138850
Desc
Variant0002
Relatedalso
ClinVar
Risk rs104893837(A;A)
Alt rs104893837(A;A)
Reference rs104893837(G;G)
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.68606400C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030908.25,