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rs201865159

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs201865159(C;C)
Make rs201865159(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415060
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs201865159
ebirs201865159
HLIrs201865159
Exacrs201865159
Varsomers201865159
Maprs201865159
PheGenIrs201865159
hapmaprs201865159
1000 genomesrs201865159
hgdprs201865159
ensemblrs201865159
gopubmedrs201865159
geneviewrs201865159
scholarrs201865159
googlers201865159
pharmgkbrs201865159
gwascentralrs201865159
openSNPrs201865159
23andMers201865159
23andMe allrs201865159
SNP Nexus

SNPshotrs201865159
SNPdbers201865159
MSV3drs201865159
GWAS Ctlgrs201865159
Max Magnitude0
ClinVar
Risk rs201865159(A,C;A,C)
Alt rs201865159(A,C;A,C)
Reference rs201865159(G;G)
Significance Probable-Pathogenic
Disease Primary dilated cardiomyopathy Dilated cardiomyopathy
Variation info
Gene MYH7 MHRT
CLNDBN Primary dilated cardiomyopathy Dilated cardiomyopathy
Reversed 0
HGVS NC_000014.8:g.23884269G>A
CLNSRC
CLNACC RCV000148701.1, RCV000171838.1,