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rs546586969

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs546586969(A;A)
Make rs546586969(A;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23420020
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs546586969
ebirs546586969
HLIrs546586969
Exacrs546586969
Varsomers546586969
Maprs546586969
PheGenIrs546586969
hapmaprs546586969
1000 genomesrs546586969
hgdprs546586969
ensemblrs546586969
gopubmedrs546586969
geneviewrs546586969
scholarrs546586969
googlers546586969
pharmgkbrs546586969
gwascentralrs546586969
openSNPrs546586969
23andMers546586969
23andMe allrs546586969
SNP Nexus

SNPshotrs546586969
SNPdbers546586969
MSV3drs546586969
GWAS Ctlgrs546586969
Max Magnitude0
ClinVar
Risk rs546586969(A;A)
Alt rs546586969(A;A)
Reference rs546586969(T;T)
Significance Probable-Pathogenic
Disease not provided not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not provided not specified
Reversed 0
HGVS NC_000014.8:g.23889229T>A
CLNSRC
CLNACC RCV000158610.1, RCV000223885.1,