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rs760499581

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs760499581(C;T)
Make rs760499581(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position136283904
GenePCCB
is asnp
is mentioned by
dbSNPrs760499581
ebirs760499581
HLIrs760499581
Exacrs760499581
Varsomers760499581
Maprs760499581
PheGenIrs760499581
hapmaprs760499581
1000 genomesrs760499581
hgdprs760499581
ensemblrs760499581
gopubmedrs760499581
geneviewrs760499581
scholarrs760499581
googlers760499581
pharmgkbrs760499581
gwascentralrs760499581
openSNPrs760499581
23andMers760499581
23andMe allrs760499581
SNP Nexus

SNPshotrs760499581
SNPdbers760499581
MSV3drs760499581
GWAS Ctlgrs760499581
Max Magnitude0
ClinVar
Risk rs760499581(T;T)
Alt rs760499581(T;T)
Reference rs760499581(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136002746C>T
CLNSRC
CLNACC RCV000186095.1,