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rs104893839

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs104893839(A;A)
Make rs104893839(A;C)
ReferenceGRCh38 38.1/141
Chromosome4
Position67744659
GeneGNRHR
is asnp
is mentioned by
dbSNPrs104893839
ebirs104893839
HLIrs104893839
Exacrs104893839
Varsomers104893839
Maprs104893839
PheGenIrs104893839
hapmaprs104893839
1000 genomesrs104893839
hgdprs104893839
ensemblrs104893839
gopubmedrs104893839
geneviewrs104893839
scholarrs104893839
googlers104893839
pharmgkbrs104893839
gwascentralrs104893839
openSNPrs104893839
23andMers104893839
23andMe allrs104893839
SNP Nexus

SNPshotrs104893839
SNPdbers104893839
MSV3drs104893839
GWAS Ctlgrs104893839
Max Magnitude0
OMIM138850
Desc
Variant0005
Relatedalso
ClinVar
Risk rs104893839(A;A)
Alt rs104893839(A;A)
Reference rs104893839(C;C)
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.68610377G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030911.29,