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rs59758982

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(CCCCAGCCCTCCAGGT;CCCCAGCCCTCCAGGT) 0 common in clinvar
Make rs59758982(-;-)
Make rs59758982(-;T)
Make rs59758982(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7676351
GeneTP53
is asnp
is mentioned by
dbSNPrs59758982
ebirs59758982
HLIrs59758982
Exacrs59758982
Varsomers59758982
Maprs59758982
PheGenIrs59758982
hapmaprs59758982
1000 genomesrs59758982
hgdprs59758982
ensemblrs59758982
gopubmedrs59758982
geneviewrs59758982
scholarrs59758982
googlers59758982
pharmgkbrs59758982
gwascentralrs59758982
openSNPrs59758982
23andMers59758982
23andMe allrs59758982
SNP Nexus

SNPshotrs59758982
SNPdbers59758982
MSV3drs59758982
GWAS Ctlgrs59758982
Max Magnitude0

[PMID 19471604OA-icon.png] Lack of association between p53 gene polymorphisms and primary open angle glaucoma in the Japanese population

ClinVar
Risk rs59758982(;)
Alt rs59758982(;)
Reference rs59758982(CCCCAGCCCTCCAGGT;CCCCAGCCCTCCAGGT)
Significance Non-pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000017.10:g.7579669_7579684del16
CLNSRC
CLNACC RCV000161045.1,