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rs796052019

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs796052019(A;A)
Make rs796052019(A;G)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position100157297
GenePCCA
is asnp
is mentioned by
dbSNPrs796052019
ebirs796052019
HLIrs796052019
Exacrs796052019
Varsomers796052019
Maprs796052019
PheGenIrs796052019
hapmaprs796052019
1000 genomesrs796052019
hgdprs796052019
ensemblrs796052019
gopubmedrs796052019
geneviewrs796052019
scholarrs796052019
googlers796052019
pharmgkbrs796052019
gwascentralrs796052019
openSNPrs796052019
23andMers796052019
23andMe allrs796052019
SNP Nexus

SNPshotrs796052019
SNPdbers796052019
MSV3drs796052019
GWAS Ctlgrs796052019
Max Magnitude0
ClinVar
Risk rs796052019(A;A)
Alt rs796052019(A;A)
Reference rs796052019(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene PCCA
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.100809551G>A
CLNSRC
CLNACC RCV000186085.2,