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rs797045097

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs797045097(A;A)
Make rs797045097(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23418348
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs797045097
ebirs797045097
HLIrs797045097
Exacrs797045097
Varsomers797045097
Maprs797045097
PheGenIrs797045097
hapmaprs797045097
1000 genomesrs797045097
hgdprs797045097
ensemblrs797045097
gopubmedrs797045097
geneviewrs797045097
scholarrs797045097
googlers797045097
pharmgkbrs797045097
gwascentralrs797045097
openSNPrs797045097
23andMers797045097
23andMe allrs797045097
SNP Nexus

SNPshotrs797045097
SNPdbers797045097
MSV3drs797045097
GWAS Ctlgrs797045097
Max Magnitude0
ClinVar
Risk rs797045097(A;A)
Alt rs797045097(A;A)
Reference rs797045097(G;G)
Significance Probable-Pathogenic
Disease Familial hypertrophic cardiomyopathy 1 not specified not provided
Variation info
Gene MYH7 MIR208B
CLNDBN Familial hypertrophic cardiomyopathy 1 not specified not provided
Reversed 1
HGVS NC_000014.8:g.23887557C>T
CLNSRC
CLNACC RCV000190606.2, RCV000211873.1, RCV000223729.1,