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rs730880396

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880396(C;T)
Make rs730880396(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34792203
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880396
ebirs730880396
HLIrs730880396
Exacrs730880396
Varsomers730880396
Maprs730880396
PheGenIrs730880396
hapmaprs730880396
1000 genomesrs730880396
hgdprs730880396
ensemblrs730880396
gopubmedrs730880396
geneviewrs730880396
scholarrs730880396
googlers730880396
pharmgkbrs730880396
gwascentralrs730880396
openSNPrs730880396
23andMers730880396
23andMe allrs730880396
SNP Nexus

SNPshotrs730880396
SNPdbers730880396
MSV3drs730880396
GWAS Ctlgrs730880396
Max Magnitude0
ClinVar
Risk rs730880396(T;T)
Alt rs730880396(T;T)
Reference rs730880396(C;C)
Significance Pathogenic
Disease Cardiomyopathy
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN Cardiomyopathy
Reversed 1
HGVS NC_000015.9:g.35084404G>A
CLNSRC
CLNACC RCV000157786.1,