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rs398123787

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123787(A;A)
Make rs398123787(A;G)
ReferenceGRCh38 38.1/141
Chromosome2
Position71612726
GeneDYSF
is asnp
is mentioned by
dbSNPrs398123787
ebirs398123787
HLIrs398123787
Exacrs398123787
Varsomers398123787
Maprs398123787
PheGenIrs398123787
hapmaprs398123787
1000 genomesrs398123787
hgdprs398123787
ensemblrs398123787
gopubmedrs398123787
geneviewrs398123787
scholarrs398123787
googlers398123787
pharmgkbrs398123787
gwascentralrs398123787
openSNPrs398123787
23andMers398123787
23andMe allrs398123787
SNP Nexus

SNPshotrs398123787
SNPdbers398123787
MSV3drs398123787
GWAS Ctlgrs398123787
Max Magnitude0
ClinVar
Risk rs398123787(A;A)
Alt rs398123787(A;A)
Reference rs398123787(G;G)
Significance Other
Disease not provided Limb-girdle muscular dystrophy
Variation info
Gene DYSF
CLNDBN not provided Limb-girdle muscular dystrophy, type 2B
Reversed 0
HGVS NC_000002.11:g.71839856G>A
CLNSRC HGMD
CLNACC RCV000080287.3, RCV000177998.2,