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rs540263945

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs540263945(C;G)
Make rs540263945(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23419587
GeneMIR208B, MYH7
is asnp
is mentioned by
dbSNPrs540263945
ebirs540263945
HLIrs540263945
Exacrs540263945
Varsomers540263945
Maprs540263945
PheGenIrs540263945
hapmaprs540263945
1000 genomesrs540263945
hgdprs540263945
ensemblrs540263945
gopubmedrs540263945
geneviewrs540263945
scholarrs540263945
googlers540263945
pharmgkbrs540263945
gwascentralrs540263945
openSNPrs540263945
23andMers540263945
23andMe allrs540263945
SNP Nexus

SNPshotrs540263945
SNPdbers540263945
MSV3drs540263945
GWAS Ctlgrs540263945
Max Magnitude0
ClinVar
Risk rs540263945(G,T;G,T)
Alt rs540263945(G,T;G,T)
Reference rs540263945(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene MYH7 MIR208B
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.23888796C>G
CLNSRC
CLNACC RCV000158619.1,