Have questions? Visit https://www.reddit.com/r/SNPedia

rs540263945

From SNPedia

Orientationplus
Stabilizedplus
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
dbSNP (classic)rs540263945
ClinGenrs540263945
ebirs540263945
HLIrs540263945
Exacrs540263945
Gnomadrs540263945
Varsomers540263945
LitVarrs540263945
Maprs540263945
PheGenIrs540263945
Biobankrs540263945
1000 genomesrs540263945
hgdprs540263945
ensemblrs540263945
geneviewrs540263945
scholarrs540263945
googlers540263945
pharmgkbrs540263945
gwascentralrs540263945
openSNPrs540263945
23andMers540263945
SNPshotrs540263945
SNPdbers540263945
MSV3drs540263945
GWAS Ctlgrs540263945
Max Magnitude0
ClinVar
Risk rs540263945(G;G) rs540263945(T;T)
Alt rs540263945(G;G) rs540263945(T;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,