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rs370549437

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs370549437(C;C)
Make rs370549437(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome13
Position100309876
GenePCCA
is asnp
is mentioned by
dbSNPrs370549437
ebirs370549437
HLIrs370549437
Exacrs370549437
Varsomers370549437
Maprs370549437
PheGenIrs370549437
hapmaprs370549437
1000 genomesrs370549437
hgdprs370549437
ensemblrs370549437
gopubmedrs370549437
geneviewrs370549437
scholarrs370549437
googlers370549437
pharmgkbrs370549437
gwascentralrs370549437
openSNPrs370549437
23andMers370549437
23andMe allrs370549437
SNP Nexus

SNPshotrs370549437
SNPdbers370549437
MSV3drs370549437
GWAS Ctlgrs370549437
Max Magnitude0
ClinVar
Risk rs370549437(C;C)
Alt rs370549437(C;C)
Reference rs370549437(T;T)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene PCCA
CLNDBN not provided
Reversed 0
HGVS NC_000013.10:g.100962130T>C
CLNSRC
CLNACC RCV000186082.1,