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rs398123774

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GGAGG;GGAGG) 0 common in clinvar
Make rs398123774(-;-)
Make rs398123774(-;GGAGG)
ReferenceGRCh38 38.1/141
Chromosome2
Position71561941
GeneDYSF
is asnp
is mentioned by
dbSNPrs398123774
ebirs398123774
HLIrs398123774
Exacrs398123774
Varsomers398123774
Maprs398123774
PheGenIrs398123774
hapmaprs398123774
1000 genomesrs398123774
hgdprs398123774
ensemblrs398123774
gopubmedrs398123774
geneviewrs398123774
scholarrs398123774
googlers398123774
pharmgkbrs398123774
gwascentralrs398123774
openSNPrs398123774
23andMers398123774
23andMe allrs398123774
SNP Nexus

SNPshotrs398123774
SNPdbers398123774
MSV3drs398123774
GWAS Ctlgrs398123774
Max Magnitude0
ClinVar
Risk rs398123774(;)
Alt rs398123774(;)
Reference rs398123774(GGAGG;GGAGG)
Significance Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.12:g.71561941_71561945delGGAGG
CLNSRC ClinVar
CLNACC RCV000080250.1,