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rs730880756

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880756(A;A)
Make rs730880756(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424122
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880756
ebirs730880756
HLIrs730880756
Exacrs730880756
Varsomers730880756
Maprs730880756
PheGenIrs730880756
hapmaprs730880756
1000 genomesrs730880756
hgdprs730880756
ensemblrs730880756
gopubmedrs730880756
geneviewrs730880756
scholarrs730880756
googlers730880756
pharmgkbrs730880756
gwascentralrs730880756
openSNPrs730880756
23andMers730880756
23andMe allrs730880756
SNP Nexus

SNPshotrs730880756
SNPdbers730880756
MSV3drs730880756
GWAS Ctlgrs730880756
Max Magnitude0
ClinVar
Risk rs730880756(A;A)
Alt rs730880756(A;A)
Reference rs730880756(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23893331C>T
CLNSRC
CLNACC RCV000158564.1,