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rs199476337

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs199476337(C;C)
Make rs199476337(C;T)
ReferenceGRCh38.p7 38.3/149
Chromosome3
Position8745712
GeneCAV3, SSUH2
is asnp
is mentioned by
dbSNPrs199476337
dbSNP (classic)rs199476337
ClinGenrs199476337
ebirs199476337
HLIrs199476337
Exacrs199476337
Gnomadrs199476337
Varsomers199476337
LitVarrs199476337
Maprs199476337
PheGenIrs199476337
Biobankrs199476337
1000 genomesrs199476337
hgdprs199476337
ensemblrs199476337
geneviewrs199476337
scholarrs199476337
googlers199476337
pharmgkbrs199476337
gwascentralrs199476337
openSNPrs199476337
23andMers199476337
23andMe allrs199476337
SNPshotrs199476337
SNPdbers199476337
MSV3drs199476337
GWAS Ctlgrs199476337
Max Magnitude0
ClinVar
Risk rs199476337(C;C)
Alt rs199476337(C;C)
Reference Rs199476337(T;T)
Significance Untested
Disease not provided
Variation info
Gene SSUH2 CAV3
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.8787398T>C
CLNSRC Leiden Muscular Dystrophy pages (CAV3)
CLNACC RCV000024420.1,