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rs797045900

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs797045900(A;A)
Make rs797045900(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome19
Position53882648
GenePRKCG
is asnp
is mentioned by
dbSNPrs797045900
ebirs797045900
HLIrs797045900
Exacrs797045900
Varsomers797045900
Maprs797045900
PheGenIrs797045900
hapmaprs797045900
1000 genomesrs797045900
hgdprs797045900
ensemblrs797045900
gopubmedrs797045900
geneviewrs797045900
scholarrs797045900
googlers797045900
pharmgkbrs797045900
gwascentralrs797045900
openSNPrs797045900
23andMers797045900
23andMe allrs797045900
SNP Nexus

SNPshotrs797045900
SNPdbers797045900
MSV3drs797045900
GWAS Ctlgrs797045900
Max Magnitude0
ClinVar
Risk rs797045900(A;A)
Alt rs797045900(A;A)
Reference rs797045900(T;T)
Significance Probable-Pathogenic
Disease Spinocerebellar ataxia 14
Variation info
Gene PRKCG
CLNDBN Spinocerebellar ataxia 14
Reversed 0
HGVS NC_000019.9:g.54385902T>A
CLNSRC
CLNACC RCV000194843.1,