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rs727504352

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs727504352(C;T)
Make rs727504352(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23418349
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs727504352
ebirs727504352
HLIrs727504352
Exacrs727504352
Varsomers727504352
Maprs727504352
PheGenIrs727504352
hapmaprs727504352
1000 genomesrs727504352
hgdprs727504352
ensemblrs727504352
gopubmedrs727504352
geneviewrs727504352
scholarrs727504352
googlers727504352
pharmgkbrs727504352
gwascentralrs727504352
openSNPrs727504352
23andMers727504352
23andMe allrs727504352
SNP Nexus

SNPshotrs727504352
SNPdbers727504352
MSV3drs727504352
GWAS Ctlgrs727504352
Max Magnitude0
ClinVar
Risk rs727504352(A,T;A,T)
Alt rs727504352(A,T;A,T)
Reference rs727504352(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23887558G>A
CLNSRC
CLNACC RCV000154475.2,