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rs878855337

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs878855337(C;C)
Make rs878855337(C;G)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position93132385
GeneSAMD9L
is asnp
is mentioned by
dbSNPrs878855337
ebirs878855337
HLIrs878855337
Exacrs878855337
Varsomers878855337
Maprs878855337
PheGenIrs878855337
hapmaprs878855337
1000 genomesrs878855337
hgdprs878855337
ensemblrs878855337
gopubmedrs878855337
geneviewrs878855337
scholarrs878855337
googlers878855337
pharmgkbrs878855337
gwascentralrs878855337
openSNPrs878855337
23andMers878855337
23andMe allrs878855337
SNP Nexus

SNPshotrs878855337
SNPdbers878855337
MSV3drs878855337
GWAS Ctlgrs878855337
Max Magnitude0
ClinVar
Risk rs878855337(C;C)
Alt rs878855337(C;C)
Reference rs878855337(G;G)
Significance Pathogenic
Disease Myelocerebellar disorder
Variation info
Gene SAMD9L
CLNDBN Myelocerebellar disorder
Reversed 1
HGVS NC_000007.13:g.92761698C>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000234841.1,