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rs730880906

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880906(A;A)
Make rs730880906(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome14
Position23419522
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880906
ebirs730880906
HLIrs730880906
Exacrs730880906
Varsomers730880906
Maprs730880906
PheGenIrs730880906
hapmaprs730880906
1000 genomesrs730880906
hgdprs730880906
ensemblrs730880906
gopubmedrs730880906
geneviewrs730880906
scholarrs730880906
googlers730880906
pharmgkbrs730880906
gwascentralrs730880906
openSNPrs730880906
23andMers730880906
23andMe allrs730880906
SNP Nexus

SNPshotrs730880906
SNPdbers730880906
MSV3drs730880906
GWAS Ctlgrs730880906
Max Magnitude0
ClinVar
Risk rs730880906(A;A)
Alt rs730880906(A;A)
Reference rs730880906(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23888731C>T
CLNSRC
CLNACC RCV000158860.2,