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rs879255651

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs879255651(A;A)
Make rs879255651(A;G)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position155116548
GeneMME
is asnp
is mentioned by
dbSNPrs879255651
dbSNP (classic)rs879255651
ClinGenrs879255651
ebirs879255651
HLIrs879255651
Exacrs879255651
Gnomadrs879255651
Varsomers879255651
LitVarrs879255651
Maprs879255651
PheGenIrs879255651
Biobankrs879255651
1000 genomesrs879255651
hgdprs879255651
ensemblrs879255651
geneviewrs879255651
scholarrs879255651
googlers879255651
pharmgkbrs879255651
gwascentralrs879255651
openSNPrs879255651
23andMers879255651
23andMe allrs879255651
SNPshotrs879255651
SNPdbers879255651
MSV3drs879255651
GWAS Ctlgrs879255651
Max Magnitude0
ClinVar
Risk rs879255651(A;A)
Alt rs879255651(A;A)
Reference Rs879255651(G;G)
Significance Pathogenic
Disease Spinocerebellar ataxia 43
Variation info
Gene MME
CLNDBN Spinocerebellar ataxia 43
Reversed 0
HGVS NC_000003.11:g.154834337G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000239627.2,