Have questions? Visit https://www.reddit.com/r/SNPedia

rs121909297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121909297(A;A)
Make rs121909297(A;G)
ReferenceGRCh38 38.1/141
Chromosome5
Position156759301
GeneSGCD
is asnp
is mentioned by
dbSNPrs121909297
ebirs121909297
HLIrs121909297
Exacrs121909297
Varsomers121909297
Maprs121909297
PheGenIrs121909297
hapmaprs121909297
1000 genomesrs121909297
hgdprs121909297
ensemblrs121909297
gopubmedrs121909297
geneviewrs121909297
scholarrs121909297
googlers121909297
pharmgkbrs121909297
gwascentralrs121909297
openSNPrs121909297
23andMers121909297
23andMe allrs121909297
SNP Nexus

SNPshotrs121909297
SNPdbers121909297
MSV3drs121909297
GWAS Ctlgrs121909297
Max Magnitude0
OMIM601411
Desc
Variant0004
Relatedalso
ClinVar
Risk rs121909297(A;A)
Alt rs121909297(A;A)
Reference rs121909297(G;G)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene SGCD
CLNDBN Limb-girdle muscular dystrophy, type 2F
Reversed 0
HGVS NC_000005.9:g.156186312G>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000008652.3,