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rs397515437

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs397515437(A;A)
Make rs397515437(A;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position83542270
GeneVCAN
is asnp
is mentioned by
dbSNPrs397515437
ebirs397515437
HLIrs397515437
Exacrs397515437
Varsomers397515437
Maprs397515437
PheGenIrs397515437
hapmaprs397515437
1000 genomesrs397515437
hgdprs397515437
ensemblrs397515437
gopubmedrs397515437
geneviewrs397515437
scholarrs397515437
googlers397515437
pharmgkbrs397515437
gwascentralrs397515437
openSNPrs397515437
23andMers397515437
23andMe allrs397515437
SNP Nexus

SNPshotrs397515437
SNPdbers397515437
MSV3drs397515437
GWAS Ctlgrs397515437
Max Magnitude0
ClinVar
Risk rs397515437(A;A)
Alt rs397515437(A;A)
Reference rs397515437(T;T)
Significance Pathogenic
Disease Wagner syndrome
Variation info
Gene VCAN
CLNDBN Wagner syndrome
Reversed 0
HGVS NC_000005.9:g.82838089T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000034808.29,