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rs370328209

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs370328209(C;T)
Make rs370328209(T;T)
ReferenceGRCh38 38.1/142
Chromosome14
Position23415801
GeneMYH7
is asnp
is mentioned by
dbSNPrs370328209
ebirs370328209
HLIrs370328209
Exacrs370328209
Varsomers370328209
Maprs370328209
PheGenIrs370328209
hapmaprs370328209
1000 genomesrs370328209
hgdprs370328209
ensemblrs370328209
gopubmedrs370328209
geneviewrs370328209
scholarrs370328209
googlers370328209
pharmgkbrs370328209
gwascentralrs370328209
openSNPrs370328209
23andMers370328209
23andMe allrs370328209
SNP Nexus

SNPshotrs370328209
SNPdbers370328209
MSV3drs370328209
GWAS Ctlgrs370328209
Max Magnitude0
ClinVar
Risk rs370328209(G,T;G,T)
Alt rs370328209(G,T;G,T)
Reference rs370328209(C;C)
Significance Pathogenic
Disease Myopathy not specified Primary dilated cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1 not specified Primary dilated cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23885010C>G; NC_000014.8:g.23885010C>T
CLNSRC ClinVar University of Washington
CLNACC RCV000132755.2, RCV000035943.3, RCV000148703.1,