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

rs2277984

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs2277984(A;A)
Make rs2277984(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome19
Position6679500
GeneC3
is asnp
is mentioned by
dbSNPrs2277984
dbSNP (old)rs2277984
ClinGenrs2277984
ebirs2277984
HLIrs2277984
Exacrs2277984
Gnomadrs2277984
Varsomers2277984
Maprs2277984
PheGenIrs2277984
Biobankrs2277984
1000 genomesrs2277984
hgdprs2277984
ensemblrs2277984
gopubmedrs2277984
geneviewrs2277984
scholarrs2277984
googlers2277984
pharmgkbrs2277984
gwascentralrs2277984
openSNPrs2277984
23andMers2277984
23andMe allrs2277984
SNP Nexus

SNPshotrs2277984
SNPdbers2277984
MSV3drs2277984
GWAS Ctlgrs2277984
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 26503818] Complement 3 and metabolic syndrome induced by clozapine: a cross-sectional study and retrospective cohort analysis


ClinVar
Risk rs2277984(A;A)
Alt rs2277984(A;A)
Reference Rs2277984(G;G)
Significance Non-pathogenic
Disease Macular degeneration C3 deficiency Atypical hemolytic uremic syndrome
Variation info
Gene C3
CLNDBN Macular degeneration C3 deficiency Atypical hemolytic uremic syndrome
Reversed 1
HGVS NC_000019.9:g.6679511C>T
CLNSRC
CLNACC RCV000261116.1, RCV000316465.1, RCV000389627.1,