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rs121909587

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs121909587(C;T)
Make rs121909587(T;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position121050192
GeneC5
is asnp
is mentioned by
dbSNPrs121909587
ebirs121909587
HLIrs121909587
Exacrs121909587
Varsomers121909587
Maprs121909587
PheGenIrs121909587
hapmaprs121909587
1000 genomesrs121909587
hgdprs121909587
ensemblrs121909587
gopubmedrs121909587
geneviewrs121909587
scholarrs121909587
googlers121909587
pharmgkbrs121909587
gwascentralrs121909587
openSNPrs121909587
23andMers121909587
23andMe allrs121909587
SNP Nexus

SNPshotrs121909587
SNPdbers121909587
MSV3drs121909587
GWAS Ctlgrs121909587
GMAF0.0004591
Max Magnitude0
OMIM120900
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121909587(T;T)
Alt rs121909587(T;T)
Reference rs121909587(C;C)
Significance Pathogenic
Disease Leiner disease
Variation info
Gene C5
CLNDBN Leiner disease
Reversed 1
HGVS NC_000009.11:g.123812470G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000018578.27,