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rs138268837

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs138268837(C;G)
Make rs138268837(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome2
Position71612672
GeneDYSF
is asnp
is mentioned by
dbSNPrs138268837
dbSNP (classic)rs138268837
ClinGenrs138268837
ebirs138268837
HLIrs138268837
Exacrs138268837
Gnomadrs138268837
Varsomers138268837
LitVarrs138268837
Maprs138268837
PheGenIrs138268837
Biobankrs138268837
1000 genomesrs138268837
hgdprs138268837
ensemblrs138268837
geneviewrs138268837
scholarrs138268837
googlers138268837
pharmgkbrs138268837
gwascentralrs138268837
openSNPrs138268837
23andMers138268837
23andMe allrs138268837
SNPshotrs138268837
SNPdbers138268837
MSV3drs138268837
GWAS Ctlgrs138268837
Max Magnitude0
ClinVar
Risk rs138268837(A;A) rs138268837(G;G)
Alt rs138268837(A;A) rs138268837(G;G)
Reference Rs138268837(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DYSF
CLNDBN not provided
Reversed 0
HGVS NC_000002.11:g.71839802C>G
CLNSRC
CLNACC RCV000494287.1,