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rs587779395

From SNPedia

Orientationminus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs587779395(-;AGA)
Make rs587779395(AGA;AGA)
ReferenceGRCh38.p2 38.2/144
Chromosome14
Position23415475
GeneMHRT, MYH7
is asnp
is mentioned by
dbSNPrs587779395
ClinGenrs587779395
ebirs587779395
HLIrs587779395
Exacrs587779395
Varsomers587779395
Maprs587779395
PheGenIrs587779395
hapmaprs587779395
1000 genomesrs587779395
hgdprs587779395
ensemblrs587779395
gopubmedrs587779395
geneviewrs587779395
scholarrs587779395
googlers587779395
pharmgkbrs587779395
gwascentralrs587779395
openSNPrs587779395
23andMers587779395
23andMe allrs587779395
SNP Nexus

SNPshotrs587779395
SNPdbers587779395
MSV3drs587779395
GWAS Ctlgrs587779395
Max Magnitude0
ClinVar
Risk rs587779395(AGA;AGA)
Alt rs587779395(AGA;AGA)
Reference Rs587779395(;)
Significance Pathogenic
Disease Myopathy
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1
Reversed 1
HGVS NC_000014.8:g.23884685_23884687dupTCT
CLNSRC
CLNACC RCV000132757.2,