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rs730880818

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880818(A;A)
Make rs730880818(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415144
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs730880818
ebirs730880818
HLIrs730880818
Exacrs730880818
Varsomers730880818
Maprs730880818
PheGenIrs730880818
hapmaprs730880818
1000 genomesrs730880818
hgdprs730880818
ensemblrs730880818
gopubmedrs730880818
geneviewrs730880818
scholarrs730880818
googlers730880818
pharmgkbrs730880818
gwascentralrs730880818
openSNPrs730880818
23andMers730880818
23andMe allrs730880818
SNP Nexus

SNPshotrs730880818
SNPdbers730880818
MSV3drs730880818
GWAS Ctlgrs730880818
Max Magnitude0
ClinVar
Risk rs730880818(A;A)
Alt rs730880818(A;A)
Reference rs730880818(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23884353C>T
CLNSRC
CLNACC RCV000158701.2,