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rs727504558

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs727504558(A;C)
Make rs727504558(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23424046
GeneMYH7
is asnp
is mentioned by
dbSNPrs727504558
dbSNP (old)rs727504558
ClinGenrs727504558
ebirs727504558
HLIrs727504558
Exacrs727504558
Gnomadrs727504558
Varsomers727504558
Maprs727504558
PheGenIrs727504558
Biobankrs727504558
1000 genomesrs727504558
hgdprs727504558
ensemblrs727504558
gopubmedrs727504558
geneviewrs727504558
scholarrs727504558
googlers727504558
pharmgkbrs727504558
gwascentralrs727504558
openSNPrs727504558
23andMers727504558
23andMe allrs727504558
SNP Nexus

SNPshotrs727504558
SNPdbers727504558
MSV3drs727504558
GWAS Ctlgrs727504558
Max Magnitude0
ClinVar
Risk rs727504558(C;C) rs727504558(T;T)
Alt rs727504558(C;C) rs727504558(T;T)
Reference Rs727504558(A;A)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene MYH7
CLNDBN not provided not specified
Reversed 1
HGVS NC_000014.8:g.23893255T>A; NC_000014.8:g.23893255T>G
CLNSRC
CLNACC RCV000158852.2, RCV000155723.1,