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rs28934590

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in complete genomics
Make rs28934590(C;T)
Make rs28934590(T;T)
ReferenceGRCh38 38.1/142
Chromosome6
Position31933876
GeneC2
is asnp
is mentioned by
dbSNPrs28934590
ebirs28934590
HLIrs28934590
Exacrs28934590
Varsomers28934590
Maprs28934590
PheGenIrs28934590
hapmaprs28934590
1000 genomesrs28934590
hgdprs28934590
ensemblrs28934590
gopubmedrs28934590
geneviewrs28934590
scholarrs28934590
googlers28934590
pharmgkbrs28934590
gwascentralrs28934590
openSNPrs28934590
23andMers28934590
23andMe allrs28934590
SNP Nexus

SNPshotrs28934590
SNPdbers28934590
MSV3drs28934590
GWAS Ctlgrs28934590
Max Magnitude0
OMIM217000
DescC2 DEFICIENCY, TYPE II
Variant0002
Relatedalso


ClinVar
Risk rs28934590(T;T)
Alt rs28934590(T;T)
Reference rs28934590(C;C)
Significance Untested
Disease
Variation info
Gene C2
CLNDBN
Reversed 0
HGVS NC_000006.11:g.31901653C>T
CLNSRC
CLNACC