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rs587776846

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs587776846(C;C)
Make rs587776846(C;T)
ReferenceGRCh38 38.1/142
Chromosome9
Position121023405
GeneC5
is asnp
is mentioned by
dbSNPrs587776846
ebirs587776846
HLIrs587776846
Exacrs587776846
Varsomers587776846
Maprs587776846
PheGenIrs587776846
hapmaprs587776846
1000 genomesrs587776846
hgdprs587776846
ensemblrs587776846
gopubmedrs587776846
geneviewrs587776846
scholarrs587776846
googlers587776846
pharmgkbrs587776846
gwascentralrs587776846
openSNPrs587776846
23andMers587776846
23andMe allrs587776846
SNP Nexus

SNPshotrs587776846
SNPdbers587776846
MSV3drs587776846
GWAS Ctlgrs587776846
Max Magnitude0
ClinVar
Risk rs587776846(C;C)
Alt rs587776846(C;C)
Reference rs587776846(T;T)
Significance Pathogenic
Disease Leiner disease
Variation info
Gene C5
CLNDBN Leiner disease
Reversed 0
HGVS NC_000009.11:g.123785683T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000018581.27,