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rs45520836

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs45520836(A;A)
Make rs45520836(A;G)
ReferenceGRCh38 38.1/142
Chromosome14
Position23414074
GeneMYH7
is asnp
is mentioned by
dbSNPrs45520836
ebirs45520836
HLIrs45520836
Exacrs45520836
Varsomers45520836
Maprs45520836
PheGenIrs45520836
hapmaprs45520836
1000 genomesrs45520836
hgdprs45520836
ensemblrs45520836
gopubmedrs45520836
geneviewrs45520836
scholarrs45520836
googlers45520836
pharmgkbrs45520836
gwascentralrs45520836
openSNPrs45520836
23andMers45520836
23andMe allrs45520836
SNP Nexus

SNPshotrs45520836
SNPdbers45520836
MSV3drs45520836
GWAS Ctlgrs45520836
Max Magnitude0
ClinVar
Risk rs45520836(A;A)
Alt rs45520836(A;A)
Reference rs45520836(G;G)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7 MHRT
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23883283C>T
CLNSRC ClinVar
CLNACC RCV000035971.3,