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rs730880911

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880911(C;C)
Make rs730880911(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23417202
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880911
ebirs730880911
HLIrs730880911
Exacrs730880911
Varsomers730880911
Maprs730880911
PheGenIrs730880911
hapmaprs730880911
1000 genomesrs730880911
hgdprs730880911
ensemblrs730880911
gopubmedrs730880911
geneviewrs730880911
scholarrs730880911
googlers730880911
pharmgkbrs730880911
gwascentralrs730880911
openSNPrs730880911
23andMers730880911
23andMe allrs730880911
SNP Nexus

SNPshotrs730880911
SNPdbers730880911
MSV3drs730880911
GWAS Ctlgrs730880911
Max Magnitude0
ClinVar
Risk rs730880911(C;C)
Alt rs730880911(C;C)
Reference rs730880911(G;G)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYH7 MHRT
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23886411C>G
CLNSRC
CLNACC RCV000158866.1, RCV000219927.1,