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rs796052018

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052018(C;C)
Make rs796052018(C;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position100449297
GenePCCA
is asnp
is mentioned by
dbSNPrs796052018
ebirs796052018
HLIrs796052018
Exacrs796052018
Varsomers796052018
Maprs796052018
PheGenIrs796052018
hapmaprs796052018
1000 genomesrs796052018
hgdprs796052018
ensemblrs796052018
gopubmedrs796052018
geneviewrs796052018
scholarrs796052018
googlers796052018
pharmgkbrs796052018
gwascentralrs796052018
openSNPrs796052018
23andMers796052018
23andMe allrs796052018
SNP Nexus

SNPshotrs796052018
SNPdbers796052018
MSV3drs796052018
GWAS Ctlgrs796052018
Max Magnitude0
ClinVar
Risk rs796052018(C;C)
Alt rs796052018(C;C)
Reference rs796052018(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCCA
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.101101551G>C
CLNSRC
CLNACC RCV000186083.1,