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rs121918340

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs121918340(A;G)
Make rs121918340(G;G)
ReferenceGRCh38 38.1/141
Chromosome9
Position137449656
GeneNSMF
is asnp
is mentioned by
dbSNPrs121918340
ebirs121918340
HLIrs121918340
Exacrs121918340
Varsomers121918340
Maprs121918340
PheGenIrs121918340
hapmaprs121918340
1000 genomesrs121918340
hgdprs121918340
ensemblrs121918340
gopubmedrs121918340
geneviewrs121918340
scholarrs121918340
googlers121918340
pharmgkbrs121918340
gwascentralrs121918340
openSNPrs121918340
23andMers121918340
23andMe allrs121918340
SNP Nexus

SNPshotrs121918340
SNPdbers121918340
MSV3drs121918340
GWAS Ctlgrs121918340
Max Magnitude0
OMIM608137
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121918340(G;G)
Alt rs121918340(G;G)
Reference rs121918340(A;A)
Significance Other
Disease Hypogonadotropic hypogonadism 9 with or without anosmia
Variation info
Gene MIR7114 NSMF
CLNDBN Hypogonadotropic hypogonadism 9 with or without anosmia
Reversed 1
HGVS NC_000009.11:g.140344108T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000030872.3,