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rs796052032

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052032(C;T)
Make rs796052032(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66850112
GenePC
is asnp
is mentioned by
dbSNPrs796052032
ebirs796052032
HLIrs796052032
Exacrs796052032
Varsomers796052032
Maprs796052032
PheGenIrs796052032
hapmaprs796052032
1000 genomesrs796052032
hgdprs796052032
ensemblrs796052032
gopubmedrs796052032
geneviewrs796052032
scholarrs796052032
googlers796052032
pharmgkbrs796052032
gwascentralrs796052032
openSNPrs796052032
23andMers796052032
23andMe allrs796052032
SNP Nexus

SNPshotrs796052032
SNPdbers796052032
MSV3drs796052032
GWAS Ctlgrs796052032
Max Magnitude0
ClinVar
Risk rs796052032(T;T)
Alt rs796052032(T;T)
Reference rs796052032(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66617583G>A
CLNSRC
CLNACC RCV000186130.1,