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rs796052030

From SNPedia

Orientationminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs796052030(A;A)
Make rs796052030(A;C)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66870408
GenePC
is asnp
is mentioned by
dbSNPrs796052030
ebirs796052030
HLIrs796052030
Exacrs796052030
Varsomers796052030
Maprs796052030
PheGenIrs796052030
hapmaprs796052030
1000 genomesrs796052030
hgdprs796052030
ensemblrs796052030
gopubmedrs796052030
geneviewrs796052030
scholarrs796052030
googlers796052030
pharmgkbrs796052030
gwascentralrs796052030
openSNPrs796052030
23andMers796052030
23andMe allrs796052030
SNP Nexus

SNPshotrs796052030
SNPdbers796052030
MSV3drs796052030
GWAS Ctlgrs796052030
Max Magnitude0
ClinVar
Risk rs796052030(A;A)
Alt rs796052030(A;A)
Reference rs796052030(C;C)
Significance Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 1
HGVS NC_000011.9:g.66637879G>T
CLNSRC
CLNACC RCV000186128.1,