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rs756328339

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs756328339(A;G)
Make rs756328339(G;G)
ReferenceGRCh38.p2 38.2/144
Chromosome2
Position71570608
GeneDYSF
is asnp
is mentioned by
dbSNPrs756328339
ebirs756328339
HLIrs756328339
Exacrs756328339
Varsomers756328339
Maprs756328339
PheGenIrs756328339
hapmaprs756328339
1000 genomesrs756328339
hgdprs756328339
ensemblrs756328339
gopubmedrs756328339
geneviewrs756328339
scholarrs756328339
googlers756328339
pharmgkbrs756328339
gwascentralrs756328339
openSNPrs756328339
23andMers756328339
23andMe allrs756328339
SNP Nexus

SNPshotrs756328339
SNPdbers756328339
MSV3drs756328339
GWAS Ctlgrs756328339
Max Magnitude0
ClinVar
Risk rs756328339(G;G)
Alt rs756328339(G;G)
Reference rs756328339(A;A)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy
Variation info
Gene DYSF
CLNDBN Limb-girdle muscular dystrophy, type 2B
Reversed 0
HGVS NC_000002.11:g.71797738A>G
CLNSRC
CLNACC RCV000176934.1,