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rs730880886

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs730880886(-;-)
Make rs730880886(-;GAC)
Make rs730880886(GAC;GAC)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425780
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880886
ebirs730880886
HLIrs730880886
Exacrs730880886
Varsomers730880886
Maprs730880886
PheGenIrs730880886
hapmaprs730880886
1000 genomesrs730880886
hgdprs730880886
ensemblrs730880886
gopubmedrs730880886
geneviewrs730880886
scholarrs730880886
googlers730880886
pharmgkbrs730880886
gwascentralrs730880886
openSNPrs730880886
23andMers730880886
23andMe allrs730880886
SNP Nexus

SNPshotrs730880886
SNPdbers730880886
MSV3drs730880886
GWAS Ctlgrs730880886
Max Magnitude0
ClinVar
Risk rs730880886(GAC;GAC)
Alt rs730880886(GAC;GAC)
Reference rs730880886(;)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894989_23894990insGTC
CLNSRC
CLNACC RCV000158827.1,