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rs786205524

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs786205524(A;A)
Make rs786205524(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position71480882
GeneDYSF
is asnp
is mentioned by
dbSNPrs786205524
ebirs786205524
HLIrs786205524
Exacrs786205524
Varsomers786205524
Maprs786205524
PheGenIrs786205524
hapmaprs786205524
1000 genomesrs786205524
hgdprs786205524
ensemblrs786205524
gopubmedrs786205524
geneviewrs786205524
scholarrs786205524
googlers786205524
pharmgkbrs786205524
gwascentralrs786205524
openSNPrs786205524
23andMers786205524
23andMe allrs786205524
SNP Nexus

SNPshotrs786205524
SNPdbers786205524
MSV3drs786205524
GWAS Ctlgrs786205524
Max Magnitude0
ClinVar
Risk rs786205524(A;A)
Alt rs786205524(A;A)
Reference rs786205524(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.71708012G>A
CLNSRC
CLNACC RCV000171291.1,