Have questions? Visit https://www.reddit.com/r/SNPedia

rs2300929

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs2300929(C;C)
Make rs2300929(C;T)
ReferenceGRCh38 38.1/141
Chromosome9
Position120954562
GeneC5
is asnp
is mentioned by
dbSNPrs2300929
ebirs2300929
HLIrs2300929
Exacrs2300929
Varsomers2300929
Maprs2300929
PheGenIrs2300929
hapmaprs2300929
1000 genomesrs2300929
hgdprs2300929
ensemblrs2300929
gopubmedrs2300929
geneviewrs2300929
scholarrs2300929
googlers2300929
pharmgkbrs2300929
gwascentralrs2300929
openSNPrs2300929
23andMers2300929
23andMe allrs2300929
SNP Nexus

SNPshotrs2300929
SNPdbers2300929
MSV3drs2300929
GWAS Ctlgrs2300929
GMAF0.2089
Max Magnitude0
? (C;C) (C;T) (T;T) 28
OMIM120900
DescLIVER FIBROSIS, SUSCEPTIBILITY TO
Variant0005
Relatedalso


[PMID 17428459] Gc-globulin concentrations and C5 haplotype-tagging polymorphisms contribute to variations in serum activity of complement factor C5.


[PMID 18644651] Evaluation of complement factor 5 variants as genetic risk factors for the development of advanced fibrosis in chronic hepatitis C infection.