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rs727505026

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs727505026(A;A)
Make rs727505026(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419958
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs727505026
ebirs727505026
HLIrs727505026
Exacrs727505026
Varsomers727505026
Maprs727505026
PheGenIrs727505026
hapmaprs727505026
1000 genomesrs727505026
hgdprs727505026
ensemblrs727505026
gopubmedrs727505026
geneviewrs727505026
scholarrs727505026
googlers727505026
pharmgkbrs727505026
gwascentralrs727505026
openSNPrs727505026
23andMers727505026
23andMe allrs727505026
SNP Nexus

SNPshotrs727505026
SNPdbers727505026
MSV3drs727505026
GWAS Ctlgrs727505026
Max Magnitude0
ClinVar
Risk rs727505026(A;A)
Alt rs727505026(A;A)
Reference rs727505026(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MIR208B
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23889167C>T
CLNSRC
CLNACC RCV000156452.1,