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rs786205525

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs786205525(A;G)
Make rs786205525(G;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position71513889
GeneDYSF
is asnp
is mentioned by
dbSNPrs786205525
ebirs786205525
HLIrs786205525
Exacrs786205525
Varsomers786205525
Maprs786205525
PheGenIrs786205525
hapmaprs786205525
1000 genomesrs786205525
hgdprs786205525
ensemblrs786205525
gopubmedrs786205525
geneviewrs786205525
scholarrs786205525
googlers786205525
pharmgkbrs786205525
gwascentralrs786205525
openSNPrs786205525
23andMers786205525
23andMe allrs786205525
SNP Nexus

SNPshotrs786205525
SNPdbers786205525
MSV3drs786205525
GWAS Ctlgrs786205525
Max Magnitude0
ClinVar
Risk rs786205525(G;G)
Alt rs786205525(G;G)
Reference rs786205525(A;A)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.71741019A>G
CLNSRC
CLNACC RCV000171292.1,