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rs397517921

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs397517921(-;-)
Make rs397517921(-;A)
ReferenceGRCh38 38.1/141
Chromosome5
Position156594939
GeneSGCD
is asnp
is mentioned by
dbSNPrs397517921
ebirs397517921
HLIrs397517921
Exacrs397517921
Varsomers397517921
Maprs397517921
PheGenIrs397517921
hapmaprs397517921
1000 genomesrs397517921
hgdprs397517921
ensemblrs397517921
gopubmedrs397517921
geneviewrs397517921
scholarrs397517921
googlers397517921
pharmgkbrs397517921
gwascentralrs397517921
openSNPrs397517921
23andMers397517921
23andMe allrs397517921
SNP Nexus

SNPshotrs397517921
SNPdbers397517921
MSV3drs397517921
GWAS Ctlgrs397517921
Max Magnitude0
ClinVar
Risk rs397517921(;)
Alt rs397517921(;)
Reference rs397517921(A;A)
Significance Probable-Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene SGCD
CLNDBN Limb-girdle muscular dystrophy
Reversed 0
HGVS NC_000005.9:g.156021949delA
CLNSRC ClinVar
CLNACC RCV000041405.2,