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rs104893841

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893841(A;A)
Make rs104893841(A;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position67740526
GeneGNRHR
is asnp
is mentioned by
dbSNPrs104893841
ebirs104893841
HLIrs104893841
Exacrs104893841
Varsomers104893841
Maprs104893841
PheGenIrs104893841
hapmaprs104893841
1000 genomesrs104893841
hgdprs104893841
ensemblrs104893841
gopubmedrs104893841
geneviewrs104893841
scholarrs104893841
googlers104893841
pharmgkbrs104893841
gwascentralrs104893841
openSNPrs104893841
23andMers104893841
23andMe allrs104893841
SNP Nexus

SNPshotrs104893841
SNPdbers104893841
MSV3drs104893841
GWAS Ctlgrs104893841
Max Magnitude0
OMIM138850
Desc
Variant0007
Relatedalso
ClinVar
Risk rs104893841(A;A)
Alt rs104893841(A;A)
Reference rs104893841(T;T)
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.68606244A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030913.29,