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rs730880773

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880773(A;A)
Make rs730880773(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23420230
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880773
ebirs730880773
HLIrs730880773
Exacrs730880773
Varsomers730880773
Maprs730880773
PheGenIrs730880773
hapmaprs730880773
1000 genomesrs730880773
hgdprs730880773
ensemblrs730880773
gopubmedrs730880773
geneviewrs730880773
scholarrs730880773
googlers730880773
pharmgkbrs730880773
gwascentralrs730880773
openSNPrs730880773
23andMers730880773
23andMe allrs730880773
SNP Nexus

SNPshotrs730880773
SNPdbers730880773
MSV3drs730880773
GWAS Ctlgrs730880773
Max Magnitude0
ClinVar
Risk rs730880773(A;A)
Alt rs730880773(A;A)
Reference rs730880773(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23889439C>T
CLNSRC
CLNACC RCV000158604.1,