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rs139222507

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs139222507(G;T)
Make rs139222507(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415249
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs139222507
ebirs139222507
HLIrs139222507
Exacrs139222507
Varsomers139222507
Maprs139222507
PheGenIrs139222507
hapmaprs139222507
1000 genomesrs139222507
hgdprs139222507
ensemblrs139222507
gopubmedrs139222507
geneviewrs139222507
scholarrs139222507
googlers139222507
pharmgkbrs139222507
gwascentralrs139222507
openSNPrs139222507
23andMers139222507
23andMe allrs139222507
SNP Nexus

SNPshotrs139222507
SNPdbers139222507
MSV3drs139222507
GWAS Ctlgrs139222507
Max Magnitude0
ClinVar
Risk rs139222507(T;T)
Alt rs139222507(T;T)
Reference rs139222507(G;G)
Significance Probable-Pathogenic
Disease Primary familial hypertrophic cardiomyopathy not provided
Variation info
Gene MYH7 MHRT
CLNDBN Primary familial hypertrophic cardiomyopathy not provided
Reversed 0
HGVS NC_000014.8:g.23884458G>T
CLNSRC
CLNACC RCV000148702.1, RCV000223890.1,