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rs556401323

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs556401323(C;T)
Make rs556401323(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome11
Position126338325
GeneDCPS
is asnp
is mentioned by
dbSNPrs556401323
dbSNP (classic)rs556401323
ClinGenrs556401323
ebirs556401323
HLIrs556401323
Exacrs556401323
Gnomadrs556401323
Varsomers556401323
LitVarrs556401323
Maprs556401323
PheGenIrs556401323
Biobankrs556401323
1000 genomesrs556401323
hgdprs556401323
ensemblrs556401323
geneviewrs556401323
scholarrs556401323
googlers556401323
pharmgkbrs556401323
gwascentralrs556401323
openSNPrs556401323
23andMers556401323
SNPshotrs556401323
SNPdbers556401323
MSV3drs556401323
GWAS Ctlgrs556401323
Max Magnitude0
ClinVar
Risk rs556401323(T;T)
Alt rs556401323(T;T)
Reference Rs556401323(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene DCPS
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.126208220C>T
CLNSRC
CLNACC RCV000492945.1,