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rs864309744

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864309744(A;A)
Make rs864309744(A;T)
ReferenceGRCh38.p2 38.2/146
Chromosome5
Position83537001
GeneLOC105379054, VCAN
is asnp
is mentioned by
dbSNPrs864309744
ebirs864309744
HLIrs864309744
Exacrs864309744
Varsomers864309744
Maprs864309744
PheGenIrs864309744
hapmaprs864309744
1000 genomesrs864309744
hgdprs864309744
ensemblrs864309744
gopubmedrs864309744
geneviewrs864309744
scholarrs864309744
googlers864309744
pharmgkbrs864309744
gwascentralrs864309744
openSNPrs864309744
23andMers864309744
23andMe allrs864309744
SNP Nexus

SNPshotrs864309744
SNPdbers864309744
MSV3drs864309744
GWAS Ctlgrs864309744
Max Magnitude0
ClinVar
Risk rs864309744(A;A)
Alt rs864309744(A;A)
Reference rs864309744(T;T)
Significance Pathogenic
Disease Wagner syndrome
Variation info
Gene VCAN
CLNDBN Wagner syndrome
Reversed 0
HGVS NC_000005.9:g.82832820T>A
CLNSRC
CLNACC RCV000203372.1,