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rs727502798

From SNPedia

Orientationminus
Geno Mag Summary
(ACA;ACA) 0 common in clinvar
Make rs727502798(-;-)
Make rs727502798(-;ACA)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position69119250
GeneLMOD3
is asnp
is mentioned by
dbSNPrs727502798
ebirs727502798
HLIrs727502798
Exacrs727502798
Varsomers727502798
Maprs727502798
PheGenIrs727502798
hapmaprs727502798
1000 genomesrs727502798
hgdprs727502798
ensemblrs727502798
gopubmedrs727502798
geneviewrs727502798
scholarrs727502798
googlers727502798
pharmgkbrs727502798
gwascentralrs727502798
openSNPrs727502798
23andMers727502798
23andMe allrs727502798
SNP Nexus

SNPshotrs727502798
SNPdbers727502798
MSV3drs727502798
GWAS Ctlgrs727502798
Max Magnitude0
ClinVar
Risk rs727502798(;)
Alt rs727502798(;)
Reference rs727502798(ACA;ACA)
Significance Pathogenic
Disease Nemaline myopathy 10
Variation info
Gene LMOD3
CLNDBN Nemaline myopathy 10
Reversed 1
HGVS NC_000003.11:g.69168401_69168403delTGT
CLNSRC OMIM Allelic Variant
CLNACC RCV000149596.4,