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rs61094188

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs61094188(C;T)
Make rs61094188(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome1
Position156136257
GeneLMNA
is asnp
is mentioned by
dbSNPrs61094188
ebirs61094188
HLIrs61094188
Exacrs61094188
Varsomers61094188
Maprs61094188
PheGenIrs61094188
hapmaprs61094188
1000 genomesrs61094188
hgdprs61094188
ensemblrs61094188
gopubmedrs61094188
geneviewrs61094188
scholarrs61094188
googlers61094188
pharmgkbrs61094188
gwascentralrs61094188
openSNPrs61094188
23andMers61094188
23andMe allrs61094188
SNP Nexus

SNPshotrs61094188
SNPdbers61094188
MSV3drs61094188
GWAS Ctlgrs61094188
Max Magnitude0
ClinVar
Risk rs61094188(T;T)
Alt rs61094188(T;T)
Reference rs61094188(C;C)
Significance Untested
Disease not specified not provided Ventricular tachycardia Emery-Dreifuss muscular dystrophy
Variation info
Gene LMNA
CLNDBN not specified not provided Ventricular tachycardia, catecholaminergic polymorphic, 1 Emery-Dreifuss muscular dystrophy
Reversed 0
HGVS NC_000001.10:g.156106048C>T
CLNSRC
CLNACC RCV000041313.2, RCV000057258.3, RCV000157295.1, RCV000172002.2,