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rs786205632

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs786205632(-;-)
Make rs786205632(-;C)
ReferenceGRCh38.p2 38.2/146
Chromosome2
Position71539192
GeneDYSF
is asnp
is mentioned by
dbSNPrs786205632
ebirs786205632
HLIrs786205632
Exacrs786205632
Varsomers786205632
Maprs786205632
PheGenIrs786205632
hapmaprs786205632
1000 genomesrs786205632
hgdprs786205632
ensemblrs786205632
gopubmedrs786205632
geneviewrs786205632
scholarrs786205632
googlers786205632
pharmgkbrs786205632
gwascentralrs786205632
openSNPrs786205632
23andMers786205632
23andMe allrs786205632
SNP Nexus

SNPshotrs786205632
SNPdbers786205632
MSV3drs786205632
GWAS Ctlgrs786205632
Max Magnitude0
ClinVar
Risk rs786205632(;)
Alt rs786205632(;)
Reference rs786205632(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.71766322delC
CLNSRC
CLNACC RCV000171494.1,