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

rs45611033

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs45611033(C;T)
Make rs45611033(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23422292
GeneMYH7
is asnp
is mentioned by
dbSNPrs45611033
ebirs45611033
HLIrs45611033
Exacrs45611033
Varsomers45611033
Maprs45611033
PheGenIrs45611033
hapmaprs45611033
1000 genomesrs45611033
hgdprs45611033
ensemblrs45611033
gopubmedrs45611033
geneviewrs45611033
scholarrs45611033
googlers45611033
pharmgkbrs45611033
gwascentralrs45611033
openSNPrs45611033
23andMers45611033
23andMe allrs45611033
SNP Nexus

SNPshotrs45611033
SNPdbers45611033
MSV3drs45611033
GWAS Ctlgrs45611033
Max Magnitude0
ClinVar
Risk rs45611033(T;T)
Alt rs45611033(T;T)
Reference rs45611033(C;C)
Significance Pathogenic
Disease not specified
Variation info
Gene MYH7
CLNDBN not specified
Reversed 1
HGVS NC_000014.8:g.23891501G>A
CLNSRC
CLNACC RCV000154366.2,