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rs104893843

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893843(A;A)
Make rs104893843(A;T)
ReferenceGRCh38 38.1/141
Chromosome4
Position67754306
GeneGNRHR
is asnp
is mentioned by
dbSNPrs104893843
ebirs104893843
HLIrs104893843
Exacrs104893843
Varsomers104893843
Maprs104893843
PheGenIrs104893843
hapmaprs104893843
1000 genomesrs104893843
hgdprs104893843
ensemblrs104893843
gopubmedrs104893843
geneviewrs104893843
scholarrs104893843
googlers104893843
pharmgkbrs104893843
gwascentralrs104893843
openSNPrs104893843
23andMers104893843
23andMe allrs104893843
SNP Nexus

SNPshotrs104893843
SNPdbers104893843
MSV3drs104893843
GWAS Ctlgrs104893843
Max Magnitude0
OMIM138850
Desc
Variant0009
Relatedalso
ClinVar
Risk rs104893843(A;A)
Alt rs104893843(A;A)
Reference rs104893843(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.68620024A>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030915.29,