Have questions? Visit https://www.reddit.com/r/SNPedia

rs201744589

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs201744589(C;T)
Make rs201744589(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position7673728
GeneTP53
is asnp
is mentioned by
dbSNPrs201744589
ebirs201744589
HLIrs201744589
Exacrs201744589
Varsomers201744589
Maprs201744589
PheGenIrs201744589
hapmaprs201744589
1000 genomesrs201744589
hgdprs201744589
ensemblrs201744589
gopubmedrs201744589
geneviewrs201744589
scholarrs201744589
googlers201744589
pharmgkbrs201744589
gwascentralrs201744589
openSNPrs201744589
23andMers201744589
23andMe allrs201744589
SNP Nexus

SNPshotrs201744589
SNPdbers201744589
MSV3drs201744589
GWAS Ctlgrs201744589
Max Magnitude0
ClinVar
Risk rs201744589(A,T;A,T)
Alt rs201744589(A,T;A,T)
Reference rs201744589(C;C)
Significance Pathogenic
Disease not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Variation info
Gene TP53
CLNDBN not provided Tumor susceptibility linked to germline BAP1 mutations Hereditary cancer-predisposing syndrome Li-Fraumeni syndrome
Reversed 0
HGVS NC_000017.10:g.7577046C>A; NC_000017.10:g.7577046C>T
CLNSRC HGMD
CLNACC RCV000079204.4, RCV000216964.1, RCV000130033.2, RCV000206802.2,