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rs371610471

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs371610471(C;T)
Make rs371610471(T;T)
ReferenceGRCh38.p2 38.2/144
Chromosome3
Position136327158
GenePCCB
is asnp
is mentioned by
dbSNPrs371610471
ebirs371610471
HLIrs371610471
Exacrs371610471
Varsomers371610471
Maprs371610471
PheGenIrs371610471
hapmaprs371610471
1000 genomesrs371610471
hgdprs371610471
ensemblrs371610471
gopubmedrs371610471
geneviewrs371610471
scholarrs371610471
googlers371610471
pharmgkbrs371610471
gwascentralrs371610471
openSNPrs371610471
23andMers371610471
23andMe allrs371610471
SNP Nexus

SNPshotrs371610471
SNPdbers371610471
MSV3drs371610471
GWAS Ctlgrs371610471
Max Magnitude0
ClinVar
Risk rs371610471(T;T)
Alt rs371610471(T;T)
Reference rs371610471(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCB
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.136046000C>A
CLNSRC
CLNACC RCV000186090.1,