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rs730880917

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880917(C;C)
Make rs730880917(C;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415156
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880917
ebirs730880917
HLIrs730880917
Exacrs730880917
Varsomers730880917
Maprs730880917
PheGenIrs730880917
hapmaprs730880917
1000 genomesrs730880917
hgdprs730880917
ensemblrs730880917
gopubmedrs730880917
geneviewrs730880917
scholarrs730880917
googlers730880917
pharmgkbrs730880917
gwascentralrs730880917
openSNPrs730880917
23andMers730880917
23andMe allrs730880917
SNP Nexus

SNPshotrs730880917
SNPdbers730880917
MSV3drs730880917
GWAS Ctlgrs730880917
Max Magnitude0
ClinVar
Risk rs730880917(C;C)
Alt rs730880917(C;C)
Reference rs730880917(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23884365C>G
CLNSRC
CLNACC RCV000158873.1,