Have questions? Visit https://www.reddit.com/r/SNPedia

rs1057519132

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519132(-;-)
Make rs1057519132(-;T)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position71664401
GeneDYSF
is asnp
is mentioned by
dbSNPrs1057519132
dbSNP (old)rs1057519132
ClinGenrs1057519132
ebirs1057519132
HLIrs1057519132
Exacrs1057519132
Gnomadrs1057519132
Varsomers1057519132
Maprs1057519132
PheGenIrs1057519132
Biobankrs1057519132
1000 genomesrs1057519132
hgdprs1057519132
ensemblrs1057519132
gopubmedrs1057519132
geneviewrs1057519132
scholarrs1057519132
googlers1057519132
pharmgkbrs1057519132
gwascentralrs1057519132
openSNPrs1057519132
23andMers1057519132
23andMe allrs1057519132
SNPshotrs1057519132
SNPdbers1057519132
MSV3drs1057519132
GWAS Ctlgrs1057519132
Max Magnitude0
ClinVar
Risk rs1057519132(-;-)
Alt rs1057519132(-;-)
Reference Rs1057519132(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.71891531delT
CLNSRC
CLNACC RCV000416117.2,