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rs369958038

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs369958038(A;A)
Make rs369958038(A;C)
ReferenceGRCh38 38.1/142
Chromosome20
Position5115472
GenePCNA
is asnp
is mentioned by
dbSNPrs369958038
ebirs369958038
HLIrs369958038
Exacrs369958038
Varsomers369958038
Maprs369958038
PheGenIrs369958038
hapmaprs369958038
1000 genomesrs369958038
hgdprs369958038
ensemblrs369958038
gopubmedrs369958038
geneviewrs369958038
scholarrs369958038
googlers369958038
pharmgkbrs369958038
gwascentralrs369958038
openSNPrs369958038
23andMers369958038
23andMe allrs369958038
SNP Nexus

SNPshotrs369958038
SNPdbers369958038
MSV3drs369958038
GWAS Ctlgrs369958038
Max Magnitude0
ClinVar
Risk rs369958038(A;A)
Alt rs369958038(A;A)
Reference rs369958038(C;C)
Significance Pathogenic
Disease Ataxia-telangiectasia-like disorder 2
Variation info
Gene PCNA
CLNDBN Ataxia-telangiectasia-like disorder 2
Reversed 0
HGVS NC_000020.10:g.5096118C>A
CLNSRC OMIM Allelic Variant
CLNACC RCV000132551.2,