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rs730880785

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs730880785(A;A)
Make rs730880785(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419266
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880785
ebirs730880785
HLIrs730880785
Exacrs730880785
Varsomers730880785
Maprs730880785
PheGenIrs730880785
hapmaprs730880785
1000 genomesrs730880785
hgdprs730880785
ensemblrs730880785
gopubmedrs730880785
geneviewrs730880785
scholarrs730880785
googlers730880785
pharmgkbrs730880785
gwascentralrs730880785
openSNPrs730880785
23andMers730880785
23andMe allrs730880785
SNP Nexus

SNPshotrs730880785
SNPdbers730880785
MSV3drs730880785
GWAS Ctlgrs730880785
Max Magnitude0
ClinVar
Risk rs730880785(A;A)
Alt rs730880785(A;A)
Reference rs730880785(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23888475C>T
CLNSRC
CLNACC RCV000158623.2,