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rs267607618

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607618(C;T)
Make rs267607618(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156136350
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607618
ebirs267607618
HLIrs267607618
Exacrs267607618
Varsomers267607618
Maprs267607618
PheGenIrs267607618
hapmaprs267607618
1000 genomesrs267607618
hgdprs267607618
ensemblrs267607618
gopubmedrs267607618
geneviewrs267607618
scholarrs267607618
googlers267607618
pharmgkbrs267607618
gwascentralrs267607618
openSNPrs267607618
23andMers267607618
23andMe allrs267607618
SNP Nexus

SNPshotrs267607618
SNPdbers267607618
MSV3drs267607618
GWAS Ctlgrs267607618
Max Magnitude0
ClinVar
Risk rs267607618(T;T)
Alt rs267607618(T;T)
Reference rs267607618(C;C)
Significance Pathogenic
Disease not provided Primary dilated cardiomyopathy Charcot-Marie-Tooth disease
Variation info
Gene LMNA
CLNDBN not provided Primary dilated cardiomyopathy Charcot-Marie-Tooth disease, type 2
Reversed 0
HGVS NC_000001.10:g.156106141C>T
CLNSRC
CLNACC RCV000057263.1, RCV000216125.1, RCV000230676.1,