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rs1057517881

From SNPedia
Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057517881(C;G)
Make rs1057517881(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome14
Position23418388
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs1057517881
dbSNP (old)rs1057517881
ClinGenrs1057517881
ebirs1057517881
HLIrs1057517881
Exacrs1057517881
Gnomadrs1057517881
Varsomers1057517881
Maprs1057517881
PheGenIrs1057517881
Biobankrs1057517881
1000 genomesrs1057517881
hgdprs1057517881
ensemblrs1057517881
gopubmedrs1057517881
geneviewrs1057517881
scholarrs1057517881
googlers1057517881
pharmgkbrs1057517881
gwascentralrs1057517881
openSNPrs1057517881
23andMers1057517881
23andMe allrs1057517881
SNPshotrs1057517881
SNPdbers1057517881
MSV3drs1057517881
GWAS Ctlgrs1057517881
Max Magnitude0
ClinVar
Risk rs1057517881(G;G)
Alt rs1057517881(G;G)
Reference Rs1057517881(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23887597G>C
CLNSRC
CLNACC RCV000412792.1,