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rs878855234

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs878855234(C;T)
Make rs878855234(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156135304
GeneLMNA
is asnp
is mentioned by
dbSNPrs878855234
ebirs878855234
HLIrs878855234
Exacrs878855234
Varsomers878855234
Maprs878855234
PheGenIrs878855234
hapmaprs878855234
1000 genomesrs878855234
hgdprs878855234
ensemblrs878855234
gopubmedrs878855234
geneviewrs878855234
scholarrs878855234
googlers878855234
pharmgkbrs878855234
gwascentralrs878855234
openSNPrs878855234
23andMers878855234
23andMe allrs878855234
SNP Nexus

SNPshotrs878855234
SNPdbers878855234
MSV3drs878855234
GWAS Ctlgrs878855234
Max Magnitude0
ClinVar
Risk rs878855234(T;T)
Alt rs878855234(T;T)
Reference rs878855234(C;C)
Significance Pathogenic
Disease Charcot-Marie-Tooth disease
Variation info
Gene LMNA
CLNDBN Charcot-Marie-Tooth disease, type 2
Reversed 0
HGVS NC_000001.10:g.156105095C>T
CLNSRC
CLNACC RCV000230197.1,