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rs539290591

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs539290591(A;A)
Make rs539290591(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23413788
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs539290591
ebirs539290591
HLIrs539290591
Exacrs539290591
Varsomers539290591
Maprs539290591
PheGenIrs539290591
hapmaprs539290591
1000 genomesrs539290591
hgdprs539290591
ensemblrs539290591
gopubmedrs539290591
geneviewrs539290591
scholarrs539290591
googlers539290591
pharmgkbrs539290591
gwascentralrs539290591
openSNPrs539290591
23andMers539290591
23andMe allrs539290591
SNP Nexus

SNPshotrs539290591
SNPdbers539290591
MSV3drs539290591
GWAS Ctlgrs539290591
Max Magnitude0
ClinVar
Risk rs539290591(A,T;A,T)
Alt rs539290591(A,T;A,T)
Reference rs539290591(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene MYH7 MHRT
CLNDBN not provided
Reversed 0
HGVS NC_000014.8:g.23882997G>A
CLNSRC
CLNACC RCV000158717.1,