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rs267607617

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607617(C;T)
Make rs267607617(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156136027
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607617
ebirs267607617
HLIrs267607617
Exacrs267607617
Varsomers267607617
Maprs267607617
PheGenIrs267607617
hapmaprs267607617
1000 genomesrs267607617
hgdprs267607617
ensemblrs267607617
gopubmedrs267607617
geneviewrs267607617
scholarrs267607617
googlers267607617
pharmgkbrs267607617
gwascentralrs267607617
openSNPrs267607617
23andMers267607617
23andMe allrs267607617
SNP Nexus

SNPshotrs267607617
SNPdbers267607617
MSV3drs267607617
GWAS Ctlgrs267607617
Max Magnitude0
ClinVar
Risk rs267607617(G,T;G,T)
Alt rs267607617(G,T;G,T)
Reference rs267607617(C;C)
Significance Pathogenic
Disease not provided Charcot-Marie-Tooth disease
Variation info
Gene LMNA
CLNDBN not provided Charcot-Marie-Tooth disease, type 2
Reversed 0
HGVS NC_000001.10:g.156105818C>T
CLNSRC
CLNACC RCV000057223.1, RCV000233611.1,