Have questions? Visit https://www.reddit.com/r/SNPedia

rs727503258

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727503258(C;G)
Make rs727503258(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23425358
GeneMYH7
is asnp
is mentioned by
dbSNPrs727503258
ebirs727503258
HLIrs727503258
Exacrs727503258
Varsomers727503258
Maprs727503258
PheGenIrs727503258
hapmaprs727503258
1000 genomesrs727503258
hgdprs727503258
ensemblrs727503258
gopubmedrs727503258
geneviewrs727503258
scholarrs727503258
googlers727503258
pharmgkbrs727503258
gwascentralrs727503258
openSNPrs727503258
23andMers727503258
23andMe allrs727503258
SNP Nexus

SNPshotrs727503258
SNPdbers727503258
MSV3drs727503258
GWAS Ctlgrs727503258
Max Magnitude0
ClinVar
Risk rs727503258(G,T;G,T)
Alt rs727503258(G,T;G,T)
Reference rs727503258(C;C)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23894567G>A; NC_000014.8:g.23894567G>C
CLNSRC
CLNACC RCV000158529.1, RCV000151274.1,