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rs863224867

From SNPedia

Orientationplus
Make rs863224867(-;-)
Make rs863224867(-;TT)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position71590284
GeneDYSF
is asnp
is mentioned by
dbSNPrs863224867
ebirs863224867
HLIrs863224867
Exacrs863224867
Varsomers863224867
Maprs863224867
PheGenIrs863224867
hapmaprs863224867
1000 genomesrs863224867
hgdprs863224867
ensemblrs863224867
gopubmedrs863224867
geneviewrs863224867
scholarrs863224867
googlers863224867
pharmgkbrs863224867
gwascentralrs863224867
openSNPrs863224867
23andMers863224867
23andMe allrs863224867
SNP Nexus

SNPshotrs863224867
SNPdbers863224867
MSV3drs863224867
GWAS Ctlgrs863224867
Max Magnitude
ClinVar
Risk rs863224867(;)
Alt rs863224867(;)
Reference rs863224867(TT;TT)
Significance Pathogenic
Disease Limb-girdle muscular dystrophy Miyoshi muscular dystrophy 1 Myopathy
Variation info
Gene DYSF
CLNDBN Limb-girdle muscular dystrophy, type 2B Miyoshi muscular dystrophy 1 Myopathy, distal, with anterior tibial onset
Reversed 0
HGVS NC_000002.11:g.71817414_71817415delTT
CLNSRC Quest Diagnostics
CLNACC RCV000198403.1, RCV000201179.1,