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rs199870606

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs199870606(C;T)
Make rs199870606(T;T)
ReferenceGRCh38.p7 38.3/149
Chromosome2
Position71611483
GeneDYSF
is asnp
is mentioned by
dbSNPrs199870606
dbSNP (classic)rs199870606
ClinGenrs199870606
ebirs199870606
HLIrs199870606
Exacrs199870606
Gnomadrs199870606
Varsomers199870606
LitVarrs199870606
Maprs199870606
PheGenIrs199870606
Biobankrs199870606
1000 genomesrs199870606
hgdprs199870606
ensemblrs199870606
geneviewrs199870606
scholarrs199870606
googlers199870606
pharmgkbrs199870606
gwascentralrs199870606
openSNPrs199870606
23andMers199870606
23andMe allrs199870606
SNPshotrs199870606
SNPdbers199870606
MSV3drs199870606
GWAS Ctlgrs199870606
Max Magnitude0
ClinVar
Risk rs199870606(T;T)
Alt rs199870606(T;T)
Reference Rs199870606(C;C)
Significance Pathogenic
Disease not specified not provided
Variation info
Gene DYSF
CLNDBN not specified not provided
Reversed 0
HGVS NC_000002.11:g.71838613C>T
CLNSRC
CLNACC RCV000343658.2, RCV000408314.1,