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rs730880402

From SNPedia

Orientationminus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs730880402(A;A)
Make rs730880402(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome15
Position34791218
GeneACTC1, LOC101928174
is asnp
is mentioned by
dbSNPrs730880402
ebirs730880402
HLIrs730880402
Exacrs730880402
Varsomers730880402
Maprs730880402
PheGenIrs730880402
hapmaprs730880402
1000 genomesrs730880402
hgdprs730880402
ensemblrs730880402
gopubmedrs730880402
geneviewrs730880402
scholarrs730880402
googlers730880402
pharmgkbrs730880402
gwascentralrs730880402
openSNPrs730880402
23andMers730880402
23andMe allrs730880402
SNP Nexus

SNPshotrs730880402
SNPdbers730880402
MSV3drs730880402
GWAS Ctlgrs730880402
Max Magnitude0
ClinVar
Risk rs730880402(A,C;A,C)
Alt rs730880402(A,C;A,C)
Reference rs730880402(T;T)
Significance Probable-Pathogenic
Disease not provided Cardiomyopathy
Variation info
Gene ACTC1 LOC101928174 RP11-814P5.1
CLNDBN not provided Cardiomyopathy
Reversed 1
HGVS NC_000015.9:g.35083419A>G; NC_000015.9:g.35083419A>T
CLNSRC
CLNACC RCV000157797.1, RCV000157796.1,