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rs786205081

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205081(-;-)
Make rs786205081(-;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position71669673
GeneDYSF
is asnp
is mentioned by
dbSNPrs786205081
ebirs786205081
HLIrs786205081
Exacrs786205081
Varsomers786205081
Maprs786205081
PheGenIrs786205081
hapmaprs786205081
1000 genomesrs786205081
hgdprs786205081
ensemblrs786205081
gopubmedrs786205081
geneviewrs786205081
scholarrs786205081
googlers786205081
pharmgkbrs786205081
gwascentralrs786205081
openSNPrs786205081
23andMers786205081
23andMe allrs786205081
SNP Nexus

SNPshotrs786205081
SNPdbers786205081
MSV3drs786205081
GWAS Ctlgrs786205081
Max Magnitude0
ClinVar
Risk rs786205081(;)
Alt rs786205081(;)
Reference rs786205081(G;G)
Significance Pathogenic
Disease Myopathy
Variation info
Gene DYSF
CLNDBN Myopathy, distal, with anterior tibial onset
Reversed 0
HGVS NC_000002.11:g.71896803delG
CLNSRC OMIM Allelic Variant
CLNACC RCV000007048.4,