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rs104893844

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs104893844(A;A)
Make rs104893844(A;G)
ReferenceGRCh38 38.1/141
Chromosome4
Position67754068
GeneGNRHR
is asnp
is mentioned by
dbSNPrs104893844
ebirs104893844
HLIrs104893844
Exacrs104893844
Varsomers104893844
Maprs104893844
PheGenIrs104893844
hapmaprs104893844
1000 genomesrs104893844
hgdprs104893844
ensemblrs104893844
gopubmedrs104893844
geneviewrs104893844
scholarrs104893844
googlers104893844
pharmgkbrs104893844
gwascentralrs104893844
openSNPrs104893844
23andMers104893844
23andMe allrs104893844
SNP Nexus

SNPshotrs104893844
SNPdbers104893844
MSV3drs104893844
GWAS Ctlgrs104893844
Max Magnitude0
OMIM138850
Desc
Variant0010
Relatedalso
ClinVar
Risk rs104893844(A;A)
Alt rs104893844(A;A)
Reference rs104893844(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.68619786C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000030916.24,