Have questions? Visit https://www.reddit.com/r/SNPedia

rs80356814

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs80356814(C;T)
Make rs80356814(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156138697
GeneLMNA
is asnp
is mentioned by
dbSNPrs80356814
ebirs80356814
HLIrs80356814
Exacrs80356814
Varsomers80356814
Maprs80356814
PheGenIrs80356814
hapmaprs80356814
1000 genomesrs80356814
hgdprs80356814
ensemblrs80356814
gopubmedrs80356814
geneviewrs80356814
scholarrs80356814
googlers80356814
pharmgkbrs80356814
gwascentralrs80356814
openSNPrs80356814
23andMers80356814
23andMe allrs80356814
SNP Nexus

SNPshotrs80356814
SNPdbers80356814
MSV3drs80356814
GWAS Ctlgrs80356814
Max Magnitude0
ClinVar
Risk rs80356814(T;T)
Alt rs80356814(T;T)
Reference rs80356814(C;C)
Significance Pathogenic
Disease not provided Charcot-Marie-Tooth disease
Variation info
Gene LMNA
CLNDBN not provided Charcot-Marie-Tooth disease
Reversed 0
HGVS NC_000001.10:g.156108488C>T
CLNSRC
CLNACC RCV000057372.1, RCV000192236.1,