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rs398123688

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs398123688(G;T)
Make rs398123688(T;T)
ReferenceGRCh38 38.1/141
Chromosome19
Position11449338
GenePRKCSH
is asnp
is mentioned by
dbSNPrs398123688
ebirs398123688
HLIrs398123688
Exacrs398123688
Varsomers398123688
Maprs398123688
PheGenIrs398123688
hapmaprs398123688
1000 genomesrs398123688
hgdprs398123688
ensemblrs398123688
gopubmedrs398123688
geneviewrs398123688
scholarrs398123688
googlers398123688
pharmgkbrs398123688
gwascentralrs398123688
openSNPrs398123688
23andMers398123688
23andMe allrs398123688
SNP Nexus

SNPshotrs398123688
SNPdbers398123688
MSV3drs398123688
GWAS Ctlgrs398123688
Max Magnitude0
ClinVar
Risk rs398123688(T;T)
Alt rs398123688(T;T)
Reference rs398123688(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PRKCSH
CLNDBN not provided
Reversed 0
HGVS NC_000019.9:g.11560153G>T
CLNSRC ClinVar Emory University
CLNACC RCV000080024.4,