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rs761295534

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs761295534(A;A)
Make rs761295534(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome13
Position100301465
GenePCCA
is asnp
is mentioned by
dbSNPrs761295534
ebirs761295534
HLIrs761295534
Exacrs761295534
Varsomers761295534
Maprs761295534
PheGenIrs761295534
hapmaprs761295534
1000 genomesrs761295534
hgdprs761295534
ensemblrs761295534
gopubmedrs761295534
geneviewrs761295534
scholarrs761295534
googlers761295534
pharmgkbrs761295534
gwascentralrs761295534
openSNPrs761295534
23andMers761295534
23andMe allrs761295534
SNP Nexus

SNPshotrs761295534
SNPdbers761295534
MSV3drs761295534
GWAS Ctlgrs761295534
Max Magnitude0
ClinVar
Risk rs761295534(A;A)
Alt rs761295534(A;A)
Reference rs761295534(G;G)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCA
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.100953719G>T
CLNSRC
CLNACC RCV000224898.1,