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rs61672878

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs61672878(A;A)
Make rs61672878(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156136094
GeneLMNA
is asnp
is mentioned by
dbSNPrs61672878
ebirs61672878
HLIrs61672878
Exacrs61672878
Varsomers61672878
Maprs61672878
PheGenIrs61672878
hapmaprs61672878
1000 genomesrs61672878
hgdprs61672878
ensemblrs61672878
gopubmedrs61672878
geneviewrs61672878
scholarrs61672878
googlers61672878
pharmgkbrs61672878
gwascentralrs61672878
openSNPrs61672878
23andMers61672878
23andMe allrs61672878
SNP Nexus

SNPshotrs61672878
SNPdbers61672878
MSV3drs61672878
GWAS Ctlgrs61672878
Max Magnitude0
OMIM150330
Desc
Variant0017
Relatedalso


ClinVar
Risk rs61672878(A,T;A,T)
Alt rs61672878(A,T;A,T)
Reference rs61672878(G;G)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy Dilated cardiomyopathy 1A not provided not specified
Variation info
Gene LMNA
CLNDBN Limb-girdle muscular dystrophy, type 1B Dilated cardiomyopathy 1A not provided not specified
Reversed 0
HGVS NC_000001.10:g.156105885G>A; NC_000001.10:g.156105885G>T
CLNSRC OMIM Allelic Variant
CLNACC RCV000015586.26, RCV000015587.22, RCV000057235.1, RCV000057236.1, RCV000216517.1,