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rs375528540

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs375528540(C;T)
Make rs375528540(T;T)
ReferenceGRCh38.p2 38.2/146
Chromosome11
Position66851239
GenePC
is asnp
is mentioned by
dbSNPrs375528540
ebirs375528540
HLIrs375528540
Exacrs375528540
Varsomers375528540
Maprs375528540
PheGenIrs375528540
hapmaprs375528540
1000 genomesrs375528540
hgdprs375528540
ensemblrs375528540
gopubmedrs375528540
geneviewrs375528540
scholarrs375528540
googlers375528540
pharmgkbrs375528540
gwascentralrs375528540
openSNPrs375528540
23andMers375528540
23andMe allrs375528540
SNP Nexus

SNPshotrs375528540
SNPdbers375528540
MSV3drs375528540
GWAS Ctlgrs375528540
Max Magnitude0
ClinVar
Risk rs375528540(T;T)
Alt rs375528540(T;T)
Reference rs375528540(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PC
CLNDBN not provided
Reversed 0
HGVS NC_000011.9:g.66618710C>T
CLNSRC
CLNACC RCV000186119.2,