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

rs397516220

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(GAG;GAG) 0 common in clinvar
Make rs397516220(-;-)
Make rs397516220(-;GAG)
ReferenceGRCh38 38.1/141
Chromosome14
Position23416988
GeneMYH7
is asnp
is mentioned by
dbSNPrs397516220
ebirs397516220
HLIrs397516220
Exacrs397516220
Varsomers397516220
Maprs397516220
PheGenIrs397516220
hapmaprs397516220
1000 genomesrs397516220
hgdprs397516220
ensemblrs397516220
gopubmedrs397516220
geneviewrs397516220
scholarrs397516220
googlers397516220
pharmgkbrs397516220
gwascentralrs397516220
openSNPrs397516220
23andMers397516220
23andMe allrs397516220
SNP Nexus

SNPshotrs397516220
SNPdbers397516220
MSV3drs397516220
GWAS Ctlgrs397516220
Max Magnitude0
ClinVar
Risk rs397516220(;)
Alt rs397516220(;)
Reference rs397516220(GAG;GAG)
Significance Pathogenic
Disease Myopathy not provided
Variation info
Gene MYH7 MHRT
CLNDBN Myopathy, distal, 1 not provided
Reversed 1
HGVS NC_000014.8:g.23886197_23886199delCTC
CLNSRC ClinVar
CLNACC RCV000132748.4, RCV000217126.1,