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rs115407852

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs115407852(A;A)
Make rs115407852(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position71681053
GeneDYSF
is asnp
is mentioned by
dbSNPrs115407852
dbSNP (old)rs115407852
ClinGenrs115407852
ebirs115407852
HLIrs115407852
Exacrs115407852
Gnomadrs115407852
Varsomers115407852
Maprs115407852
PheGenIrs115407852
Biobankrs115407852
1000 genomesrs115407852
hgdprs115407852
ensemblrs115407852
gopubmedrs115407852
geneviewrs115407852
scholarrs115407852
googlers115407852
pharmgkbrs115407852
gwascentralrs115407852
openSNPrs115407852
23andMers115407852
23andMe allrs115407852
SNPshotrs115407852
SNPdbers115407852
MSV3drs115407852
GWAS Ctlgrs115407852
Max Magnitude0
ClinVar
Risk rs115407852(A;A)
Alt rs115407852(A;A)
Reference Rs115407852(G;G)
Significance Probable-Pathogenic
Disease not specified not provided
Variation info
Gene DYSF
CLNDBN not specified not provided
Reversed 0
HGVS NC_000002.11:g.71908183G>A
CLNSRC
CLNACC RCV000356385.1, RCV000487973.1,