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rs142191737

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs142191737(A;A)
Make rs142191737(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome1
Position156137679
GeneLMNA
is asnp
is mentioned by
dbSNPrs142191737
dbSNP (old)rs142191737
ClinGenrs142191737
ebirs142191737
HLIrs142191737
Exacrs142191737
Gnomadrs142191737
Varsomers142191737
LitVarrs142191737
Maprs142191737
PheGenIrs142191737
Biobankrs142191737
1000 genomesrs142191737
hgdprs142191737
ensemblrs142191737
gopubmedrs142191737
geneviewrs142191737
scholarrs142191737
googlers142191737
pharmgkbrs142191737
gwascentralrs142191737
openSNPrs142191737
23andMers142191737
23andMe allrs142191737
SNPshotrs142191737
SNPdbers142191737
MSV3drs142191737
GWAS Ctlgrs142191737
Max Magnitude0
ClinVar
Risk rs142191737(A;A)
Alt rs142191737(A;A)
Reference Rs142191737(G;G)
Significance Probable-Pathogenic
Disease not specified Peripheral neuropathy Charcot-Marie-Tooth disease Dilated cardiomyopathy 1S
Variation info
Gene LMNA
CLNDBN not specified Peripheral neuropathy Charcot-Marie-Tooth disease, type 2 Dilated cardiomyopathy 1S
Reversed 0
HGVS NC_000001.10:g.156107470G>A
CLNSRC
CLNACC RCV000150955.3, RCV000449630.1, RCV000468904.1, RCV000491650.1,