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rs121909298

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121909298(G;G)
Make rs121909298(G;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position156595000
GeneSGCD
is asnp
is mentioned by
dbSNPrs121909298
ebirs121909298
HLIrs121909298
Exacrs121909298
Varsomers121909298
Maprs121909298
PheGenIrs121909298
hapmaprs121909298
1000 genomesrs121909298
hgdprs121909298
ensemblrs121909298
gopubmedrs121909298
geneviewrs121909298
scholarrs121909298
googlers121909298
pharmgkbrs121909298
gwascentralrs121909298
openSNPrs121909298
23andMers121909298
23andMe allrs121909298
SNP Nexus

SNPshotrs121909298
SNPdbers121909298
MSV3drs121909298
GWAS Ctlgrs121909298
Max Magnitude0
OMIM601411
Desc
Variant0006
Relatedalso
ClinVar
Risk rs121909298(G;G)
Alt rs121909298(G;G)
Reference rs121909298(T;T)
Significance Other
Disease Dilated cardiomyopathy 1L Muscular dystrophy not specified not provided
Variation info
Gene SGCD
CLNDBN Dilated cardiomyopathy 1L Muscular dystrophy, limb-girdle, type 2F, digenic not specified not provided
Reversed 0
HGVS NC_000005.9:g.156022010T>G
CLNSRC OMIM Allelic Variant
CLNACC RCV000008654.5, RCV000008655.3, RCV000041407.2, RCV000179290.1,