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rs724159965

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs724159965(G;T)
Make rs724159965(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position69119286
GeneLMOD3
is asnp
is mentioned by
dbSNPrs724159965
ebirs724159965
HLIrs724159965
Exacrs724159965
Varsomers724159965
Maprs724159965
PheGenIrs724159965
hapmaprs724159965
1000 genomesrs724159965
hgdprs724159965
ensemblrs724159965
gopubmedrs724159965
geneviewrs724159965
scholarrs724159965
googlers724159965
pharmgkbrs724159965
gwascentralrs724159965
openSNPrs724159965
23andMers724159965
23andMe allrs724159965
SNP Nexus

SNPshotrs724159965
SNPdbers724159965
MSV3drs724159965
GWAS Ctlgrs724159965
Max Magnitude0
ClinVar
Risk rs724159965(T;T)
Alt rs724159965(T;T)
Reference rs724159965(G;G)
Significance Pathogenic
Disease Nemaline myopathy 10
Variation info
Gene LMOD3
CLNDBN Nemaline myopathy 10
Reversed 1
HGVS NC_000003.11:g.69168437C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000149599.4,