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rs878855336

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855336(A;A)
Make rs878855336(A;C)
ReferenceGRCh38.p2 38.2/147
Chromosome7
Position93133332
GeneSAMD9L
is asnp
is mentioned by
dbSNPrs878855336
ebirs878855336
HLIrs878855336
Exacrs878855336
Varsomers878855336
Maprs878855336
PheGenIrs878855336
hapmaprs878855336
1000 genomesrs878855336
hgdprs878855336
ensemblrs878855336
gopubmedrs878855336
geneviewrs878855336
scholarrs878855336
googlers878855336
pharmgkbrs878855336
gwascentralrs878855336
openSNPrs878855336
23andMers878855336
23andMe allrs878855336
SNP Nexus

SNPshotrs878855336
SNPdbers878855336
MSV3drs878855336
GWAS Ctlgrs878855336
Max Magnitude0
ClinVar
Risk rs878855336(A;A)
Alt rs878855336(A;A)
Reference rs878855336(C;C)
Significance Pathogenic
Disease Myelocerebellar disorder
Variation info
Gene SAMD9L
CLNDBN Myelocerebellar disorder
Reversed 1
HGVS NC_000007.13:g.92762645G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000234838.1,