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rs121434509

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121434509(A;A)
Make rs121434509(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position9684627
GeneMTMR14
is asnp
is mentioned by
dbSNPrs121434509
ebirs121434509
HLIrs121434509
Exacrs121434509
Varsomers121434509
Maprs121434509
PheGenIrs121434509
hapmaprs121434509
1000 genomesrs121434509
hgdprs121434509
ensemblrs121434509
gopubmedrs121434509
geneviewrs121434509
scholarrs121434509
googlers121434509
pharmgkbrs121434509
gwascentralrs121434509
openSNPrs121434509
23andMers121434509
23andMe allrs121434509
SNP Nexus

SNPshotrs121434509
SNPdbers121434509
MSV3drs121434509
GWAS Ctlgrs121434509
Max Magnitude0
OMIM611089
Desc
Variant0001
Relatedalso
ClinVar
Risk rs121434509(A;A)
Alt rs121434509(A;A)
Reference rs121434509(G;G)
Significance Other
Disease MYOPATHY
Variation info
Gene MTMR14
CLNDBN MYOPATHY, CENTRONUCLEAR, AUTOSOMAL DOMINANT, MODIFIER OF
Reversed 0
HGVS NC_000003.11:g.9726311G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000001075.3,