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rs796052029

From SNPedia

Orientationminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052029(A;A)
Make rs796052029(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66852547
GenePC
is asnp
is mentioned by
dbSNPrs796052029
ebirs796052029
HLIrs796052029
Exacrs796052029
Varsomers796052029
Maprs796052029
PheGenIrs796052029
hapmaprs796052029
1000 genomesrs796052029
hgdprs796052029
ensemblrs796052029
gopubmedrs796052029
geneviewrs796052029
scholarrs796052029
googlers796052029
pharmgkbrs796052029
gwascentralrs796052029
openSNPrs796052029
23andMers796052029
23andMe allrs796052029
SNP Nexus

SNPshotrs796052029
SNPdbers796052029
MSV3drs796052029
GWAS Ctlgrs796052029
Max Magnitude0
ClinVar
Risk rs796052029(A;A)
Alt rs796052029(A;A)
Reference rs796052029(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66620018C>T
CLNSRC
CLNACC RCV000186118.1,