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rs1057521141

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057521141(C;T)
Make rs1057521141(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position71679197
GeneDYSF
is asnp
is mentioned by
dbSNPrs1057521141
dbSNP (old)rs1057521141
ClinGenrs1057521141
ebirs1057521141
HLIrs1057521141
Exacrs1057521141
Gnomadrs1057521141
Varsomers1057521141
Maprs1057521141
PheGenIrs1057521141
Biobankrs1057521141
1000 genomesrs1057521141
hgdprs1057521141
ensemblrs1057521141
gopubmedrs1057521141
geneviewrs1057521141
scholarrs1057521141
googlers1057521141
pharmgkbrs1057521141
gwascentralrs1057521141
openSNPrs1057521141
23andMers1057521141
23andMe allrs1057521141
SNPshotrs1057521141
SNPdbers1057521141
MSV3drs1057521141
GWAS Ctlgrs1057521141
Max Magnitude0
ClinVar
Risk rs1057521141(T;T)
Alt rs1057521141(T;T)
Reference Rs1057521141(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.71906327C>T
CLNSRC
CLNACC RCV000424011.1,