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rs267607623

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607623(A;A)
Make rs267607623(A;C)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136021
GeneLMNA
is asnp
is mentioned by
dbSNPrs267607623
ebirs267607623
HLIrs267607623
Exacrs267607623
Varsomers267607623
Maprs267607623
PheGenIrs267607623
hapmaprs267607623
1000 genomesrs267607623
hgdprs267607623
ensemblrs267607623
gopubmedrs267607623
geneviewrs267607623
scholarrs267607623
googlers267607623
pharmgkbrs267607623
gwascentralrs267607623
openSNPrs267607623
23andMers267607623
23andMe allrs267607623
SNP Nexus

SNPshotrs267607623
SNPdbers267607623
MSV3drs267607623
GWAS Ctlgrs267607623
Max Magnitude0
ClinVar
Risk rs267607623(A,T;A,T)
Alt rs267607623(A,T;A,T)
Reference rs267607623(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.156105812C>A; NC_000001.10:g.156105812C>T
CLNSRC
CLNACC RCV000057222.1, RCV000182362.2, RCV000229718.1,