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rs730880779

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs730880779(C;G)
Make rs730880779(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419974
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs730880779
ebirs730880779
HLIrs730880779
Exacrs730880779
Varsomers730880779
Maprs730880779
PheGenIrs730880779
hapmaprs730880779
1000 genomesrs730880779
hgdprs730880779
ensemblrs730880779
gopubmedrs730880779
geneviewrs730880779
scholarrs730880779
googlers730880779
pharmgkbrs730880779
gwascentralrs730880779
openSNPrs730880779
23andMers730880779
23andMe allrs730880779
SNP Nexus

SNPshotrs730880779
SNPdbers730880779
MSV3drs730880779
GWAS Ctlgrs730880779
Max Magnitude0
ClinVar
Risk rs730880779(G;G)
Alt rs730880779(G;G)
Reference rs730880779(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 1
HGVS NC_000014.8:g.23889183G>C
CLNSRC
CLNACC RCV000158613.1,