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rs730880809

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880809(A;A)
Make rs730880809(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23416150
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880809
ebirs730880809
HLIrs730880809
Exacrs730880809
Varsomers730880809
Maprs730880809
PheGenIrs730880809
hapmaprs730880809
1000 genomesrs730880809
hgdprs730880809
ensemblrs730880809
gopubmedrs730880809
geneviewrs730880809
scholarrs730880809
googlers730880809
pharmgkbrs730880809
gwascentralrs730880809
openSNPrs730880809
23andMers730880809
23andMe allrs730880809
SNP Nexus

SNPshotrs730880809
SNPdbers730880809
MSV3drs730880809
GWAS Ctlgrs730880809
Max Magnitude0
ClinVar
Risk rs730880809(A;A)
Alt rs730880809(A;A)
Reference rs730880809(G;G)
Significance Pathogenic
Disease Myopathy not provided
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1 not provided
Reversed 1
HGVS NC_000014.8:g.23885359C>G; NC_000014.8:g.23885359C>T
CLNSRC
CLNACC RCV000192209.1, RCV000158670.2,