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rs724159964

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs724159964(C;T)
Make rs724159964(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position69119154
GeneLMOD3
is asnp
is mentioned by
dbSNPrs724159964
ebirs724159964
HLIrs724159964
Exacrs724159964
Varsomers724159964
Maprs724159964
PheGenIrs724159964
hapmaprs724159964
1000 genomesrs724159964
hgdprs724159964
ensemblrs724159964
gopubmedrs724159964
geneviewrs724159964
scholarrs724159964
googlers724159964
pharmgkbrs724159964
gwascentralrs724159964
openSNPrs724159964
23andMers724159964
23andMe allrs724159964
SNP Nexus

SNPshotrs724159964
SNPdbers724159964
MSV3drs724159964
GWAS Ctlgrs724159964
Max Magnitude0
ClinVar
Risk rs724159964(T;T)
Alt rs724159964(T;T)
Reference rs724159964(C;C)
Significance Pathogenic
Disease Nemaline myopathy 10
Variation info
Gene LMOD3
CLNDBN Nemaline myopathy 10
Reversed 1
HGVS NC_000003.11:g.69168305G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149597.6,