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rs59301204

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs59301204(C;C)
Make rs59301204(C;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position156135956
GeneLMNA
is asnp
is mentioned by
dbSNPrs59301204
ClinGenrs59301204
ebirs59301204
HLIrs59301204
Exacrs59301204
Varsomers59301204
Maprs59301204
PheGenIrs59301204
hapmaprs59301204
1000 genomesrs59301204
hgdprs59301204
ensemblrs59301204
gopubmedrs59301204
geneviewrs59301204
scholarrs59301204
googlers59301204
pharmgkbrs59301204
gwascentralrs59301204
openSNPrs59301204
23andMers59301204
23andMe allrs59301204
SNP Nexus

SNPshotrs59301204
SNPdbers59301204
MSV3drs59301204
GWAS Ctlgrs59301204
Max Magnitude0
ClinVar
Risk rs59301204(A;A) rs59301204(C;C)
Alt rs59301204(A;A) rs59301204(C;C)
Reference Rs59301204(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy not provided
Variation info
Gene LMNA
CLNDBN Primary dilated cardiomyopathy not provided
Reversed 0
HGVS NC_000001.10:g.156105747G>A; NC_000001.10:g.156105747G>C
CLNSRC ClinVar Epithelial Biology
CLNACC RCV000041384.2, RCV000182367.2, RCV000057496.1,