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rs1064797253

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Chromosome2
Position71664399
GeneDYSF
is asnp
is mentioned by
dbSNPrs1064797253
dbSNP (classic)rs1064797253
ClinGenrs1064797253
ebirs1064797253
HLIrs1064797253
Exacrs1064797253
Gnomadrs1064797253
Varsomers1064797253
LitVarrs1064797253
Maprs1064797253
PheGenIrs1064797253
Biobankrs1064797253
1000 genomesrs1064797253
hgdprs1064797253
ensemblrs1064797253
geneviewrs1064797253
scholarrs1064797253
googlers1064797253
pharmgkbrs1064797253
gwascentralrs1064797253
openSNPrs1064797253
23andMers1064797253
23andMe allrs1064797253
SNPshotrs1064797253
SNPdbers1064797253
MSV3drs1064797253
GWAS Ctlgrs1064797253
Max Magnitude0
ClinVar
Risk rs1064797253(-;-)
Alt rs1064797253(-;-)
Reference Rs1064797253(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.71891529delA
CLNSRC
CLNACC RCV000488297.1,