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rs727502797

From SNPedia

Orientationminus
Geno Mag Summary
(;) 0 common in clinvar
Make rs727502797(-;-)
Make rs727502797(-;C)
Make rs727502797(C;C)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position69122248
GeneLMOD3
is asnp
is mentioned by
dbSNPrs727502797
ebirs727502797
HLIrs727502797
Exacrs727502797
Varsomers727502797
Maprs727502797
PheGenIrs727502797
hapmaprs727502797
1000 genomesrs727502797
hgdprs727502797
ensemblrs727502797
gopubmedrs727502797
geneviewrs727502797
scholarrs727502797
googlers727502797
pharmgkbrs727502797
gwascentralrs727502797
openSNPrs727502797
23andMers727502797
23andMe allrs727502797
SNP Nexus

SNPshotrs727502797
SNPdbers727502797
MSV3drs727502797
GWAS Ctlgrs727502797
Max Magnitude0
ClinVar
Risk rs727502797(C;C)
Alt rs727502797(C;C)
Reference rs727502797(;)
Significance Pathogenic
Disease Nemaline myopathy 10
Variation info
Gene LMOD3
CLNDBN Nemaline myopathy 10
Reversed 1
HGVS NC_000003.11:g.69171400dupG
CLNSRC OMIM Allelic Variant
CLNACC RCV000149595.4,