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rs767325003

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767325003(A;A)
Make rs767325003(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome10
Position74112087
GeneVCL
is asnp
is mentioned by
dbSNPrs767325003
ebirs767325003
HLIrs767325003
Exacrs767325003
Varsomers767325003
Maprs767325003
PheGenIrs767325003
hapmaprs767325003
1000 genomesrs767325003
hgdprs767325003
ensemblrs767325003
gopubmedrs767325003
geneviewrs767325003
scholarrs767325003
googlers767325003
pharmgkbrs767325003
gwascentralrs767325003
openSNPrs767325003
23andMers767325003
23andMe allrs767325003
SNP Nexus

SNPshotrs767325003
SNPdbers767325003
MSV3drs767325003
GWAS Ctlgrs767325003
Max Magnitude0
ClinVar
Risk rs767325003(A;A)
Alt rs767325003(A;A)
Reference rs767325003(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VCL
CLNDBN not provided
Reversed 0
HGVS NC_000010.10:g.75871845G>A
CLNSRC
CLNACC RCV000171177.1,