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

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, VCAN-AS1
is asnp
is mentioned by
dbSNPrs397515437
dbSNP (classic)rs397515437
ClinGenrs397515437
ebirs397515437
HLIrs397515437
Exacrs397515437
Gnomadrs397515437
Varsomers397515437
LitVarrs397515437
Maprs397515437
PheGenIrs397515437
Biobankrs397515437
1000 genomesrs397515437
hgdprs397515437
ensemblrs397515437
geneviewrs397515437
scholarrs397515437
googlers397515437
pharmgkbrs397515437
gwascentralrs397515437
openSNPrs397515437
23andMers397515437
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 LOC105379054 VCAN
CLNDBN Wagner syndrome
Reversed 0
HGVS NC_000005.9:g.82838089T>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000034808.30,