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rs730880887

From SNPedia

Orientationminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs730880887(-;-)
Make rs730880887(-;GAG)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424883
GeneMYH7
is asnp
is mentioned by
dbSNPrs730880887
ebirs730880887
HLIrs730880887
Exacrs730880887
Varsomers730880887
Maprs730880887
PheGenIrs730880887
hapmaprs730880887
1000 genomesrs730880887
hgdprs730880887
ensemblrs730880887
gopubmedrs730880887
geneviewrs730880887
scholarrs730880887
googlers730880887
pharmgkbrs730880887
gwascentralrs730880887
openSNPrs730880887
23andMers730880887
23andMe allrs730880887
SNP Nexus

SNPshotrs730880887
SNPdbers730880887
MSV3drs730880887
GWAS Ctlgrs730880887
Max Magnitude0
ClinVar
Risk rs730880887(;)
Alt rs730880887(;)
Reference rs730880887(GAG;GAG)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23894092_23894094delCTC
CLNSRC
CLNACC RCV000158828.1,