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rs142881576

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142881576(A;A)
Make rs142881576(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position41159152
GeneC6, LOC105374739
is asnp
is mentioned by
dbSNPrs142881576
ebirs142881576
HLIrs142881576
Exacrs142881576
Varsomers142881576
Maprs142881576
PheGenIrs142881576
hapmaprs142881576
1000 genomesrs142881576
hgdprs142881576
ensemblrs142881576
gopubmedrs142881576
geneviewrs142881576
scholarrs142881576
googlers142881576
pharmgkbrs142881576
gwascentralrs142881576
openSNPrs142881576
23andMers142881576
23andMe allrs142881576
SNP Nexus

SNPshotrs142881576
SNPdbers142881576
MSV3drs142881576
GWAS Ctlgrs142881576
Max Magnitude0
ClinVar
Risk rs142881576(A;A)
Alt rs142881576(A;A)
Reference rs142881576(G;G)
Significance Probable-Pathogenic
Disease Complement component 6 deficiency
Variation info
Gene C6
CLNDBN Complement component 6 deficiency
Reversed 0
HGVS NC_000005.9:g.41159254G>A
CLNSRC
CLNACC RCV000190569.1,