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rs727503242

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503242(C;T)
Make rs727503242(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415047
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs727503242
ebirs727503242
HLIrs727503242
Exacrs727503242
Varsomers727503242
Maprs727503242
PheGenIrs727503242
hapmaprs727503242
1000 genomesrs727503242
hgdprs727503242
ensemblrs727503242
gopubmedrs727503242
geneviewrs727503242
scholarrs727503242
googlers727503242
pharmgkbrs727503242
gwascentralrs727503242
openSNPrs727503242
23andMers727503242
23andMe allrs727503242
SNP Nexus

SNPshotrs727503242
SNPdbers727503242
MSV3drs727503242
GWAS Ctlgrs727503242
Max Magnitude0
ClinVar
Risk rs727503242(G,T;G,T)
Alt rs727503242(G,T;G,T)
Reference rs727503242(C;C)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene MYH7 MHRT
CLNDBN not specified not provided
Reversed 1
HGVS NC_000014.8:g.23884256G>A; NC_000014.8:g.23884256G>C
CLNSRC
CLNACC RCV000151235.2, RCV000158705.2,