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rs61661343

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs61661343(C;C)
Make rs61661343(C;T)
ReferenceGRCh38.p2 38.2/147
Chromosome1
Position156130687
GeneLMNA
is asnp
is mentioned by
dbSNPrs61661343
ebirs61661343
HLIrs61661343
Exacrs61661343
Varsomers61661343
Maprs61661343
PheGenIrs61661343
hapmaprs61661343
1000 genomesrs61661343
hgdprs61661343
ensemblrs61661343
gopubmedrs61661343
geneviewrs61661343
scholarrs61661343
googlers61661343
pharmgkbrs61661343
gwascentralrs61661343
openSNPrs61661343
23andMers61661343
23andMe allrs61661343
SNP Nexus

SNPshotrs61661343
SNPdbers61661343
MSV3drs61661343
GWAS Ctlgrs61661343
Max Magnitude0
ClinVar
Risk rs61661343(C;C)
Alt rs61661343(C;C)
Reference rs61661343(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene LMNA
CLNDBN not provided
Reversed 0
HGVS NC_000001.10:g.156100478T>C
CLNSRC
CLNACC RCV000057404.2,