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rs397515438

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397515438(A;A)
Make rs397515438(A;G)
ReferenceGRCh38 38.1/141
Chromosome11
Position134145989
GeneJAM3
is asnp
is mentioned by
dbSNPrs397515438
ebirs397515438
HLIrs397515438
Exacrs397515438
Varsomers397515438
Maprs397515438
PheGenIrs397515438
hapmaprs397515438
1000 genomesrs397515438
hgdprs397515438
ensemblrs397515438
gopubmedrs397515438
geneviewrs397515438
scholarrs397515438
googlers397515438
pharmgkbrs397515438
gwascentralrs397515438
openSNPrs397515438
23andMers397515438
23andMe allrs397515438
SNP Nexus

SNPshotrs397515438
SNPdbers397515438
MSV3drs397515438
GWAS Ctlgrs397515438
Max Magnitude0
ClinVar
Risk rs397515438(A;A)
Alt rs397515438(A;A)
Reference rs397515438(G;G)
Significance Pathogenic
Disease Hemorrhagic destruction of the brain
Variation info
Gene JAM3
CLNDBN Hemorrhagic destruction of the brain, subependymal calcification, and cataracts
Reversed 0
HGVS NC_000011.9:g.134015884G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000034812.4,