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rs730880751

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880751(C;C)
Make rs730880751(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424816
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880751
ebirs730880751
HLIrs730880751
Exacrs730880751
Varsomers730880751
Maprs730880751
PheGenIrs730880751
hapmaprs730880751
1000 genomesrs730880751
hgdprs730880751
ensemblrs730880751
gopubmedrs730880751
geneviewrs730880751
scholarrs730880751
googlers730880751
pharmgkbrs730880751
gwascentralrs730880751
openSNPrs730880751
23andMers730880751
23andMe allrs730880751
SNP Nexus

SNPshotrs730880751
SNPdbers730880751
MSV3drs730880751
GWAS Ctlgrs730880751
Max Magnitude0
ClinVar
Risk rs730880751(C;C)
Alt rs730880751(C;C)
Reference rs730880751(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894025C>G
CLNSRC
CLNACC RCV000158556.1,