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rs1085307922

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome14
Position23388937
GeneMIR208A, MYH6
is asnp
is mentioned by
dbSNPrs1085307922
dbSNP (old)rs1085307922
ClinGenrs1085307922
ebirs1085307922
HLIrs1085307922
Exacrs1085307922
Gnomadrs1085307922
Varsomers1085307922
Maprs1085307922
PheGenIrs1085307922
Biobankrs1085307922
1000 genomesrs1085307922
hgdprs1085307922
ensemblrs1085307922
gopubmedrs1085307922
geneviewrs1085307922
scholarrs1085307922
googlers1085307922
pharmgkbrs1085307922
gwascentralrs1085307922
openSNPrs1085307922
23andMers1085307922
23andMe allrs1085307922
SNPshotrs1085307922
SNPdbers1085307922
MSV3drs1085307922
GWAS Ctlgrs1085307922
Max Magnitude0
ClinVar
Risk rs1085307922(T;T)
Alt rs1085307922(T;T)
Reference Rs1085307922(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH6 MIR208A
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23858146G>A
CLNSRC
CLNACC RCV000489332.1,