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rs57207746

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs57207746(A;A)
Make rs57207746(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156134860
GeneLMNA
is asnp
is mentioned by
dbSNPrs57207746
ebirs57207746
HLIrs57207746
Exacrs57207746
Varsomers57207746
Maprs57207746
PheGenIrs57207746
hapmaprs57207746
1000 genomesrs57207746
hgdprs57207746
ensemblrs57207746
gopubmedrs57207746
geneviewrs57207746
scholarrs57207746
googlers57207746
pharmgkbrs57207746
gwascentralrs57207746
openSNPrs57207746
23andMers57207746
23andMe allrs57207746
SNP Nexus

SNPshotrs57207746
SNPdbers57207746
MSV3drs57207746
GWAS Ctlgrs57207746
Max Magnitude0
ClinVar
Risk rs57207746(A;A)
Alt rs57207746(A;A)
Reference rs57207746(G;G)
Significance Probable-Pathogenic
Disease not provided Benign scapuloperoneal muscular dystrophy with cardiomyopathy
Variation info
Gene LMNA
CLNDBN not provided Benign scapuloperoneal muscular dystrophy with cardiomyopathy
Reversed 0
HGVS NC_000001.10:g.156104651G>A
CLNSRC Quest Diagnostics
CLNACC RCV000057445.1, RCV000201054.1,