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rs57077886

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs57077886(C;T)
Make rs57077886(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome1
Position156114947
GeneLMNA
is asnp
is mentioned by
dbSNPrs57077886
ebirs57077886
HLIrs57077886
Exacrs57077886
Varsomers57077886
Maprs57077886
PheGenIrs57077886
hapmaprs57077886
1000 genomesrs57077886
hgdprs57077886
ensemblrs57077886
gopubmedrs57077886
geneviewrs57077886
scholarrs57077886
googlers57077886
pharmgkbrs57077886
gwascentralrs57077886
openSNPrs57077886
23andMers57077886
23andMe allrs57077886
SNP Nexus

SNPshotrs57077886
SNPdbers57077886
MSV3drs57077886
GWAS Ctlgrs57077886
Max Magnitude0
ClinVar
Risk rs57077886(T;T)
Alt rs57077886(T;T)
Reference rs57077886(C;C)
Significance Pathogenic
Disease Dilated cardiomyopathy 1A not provided
Variation info
Gene LMNA
CLNDBN Dilated cardiomyopathy 1A not provided
Reversed 0
HGVS NC_000001.10:g.156084738C>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015599.25, RCV000057387.2,