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rs587781987

From SNPedia

Orientationminus
Geno Mag Summary
(TTTGAGGTGC;TTTGAGGTGC) 0 common in clinvar
Make rs587781987(-;-)
Make rs587781987(-;TTTGAGGTGC)
ReferenceGRCh38.p2 38.2/144
Chromosome17
Position7673803
GeneTP53
is asnp
is mentioned by
dbSNPrs587781987
ebirs587781987
HLIrs587781987
Exacrs587781987
Varsomers587781987
Maprs587781987
PheGenIrs587781987
hapmaprs587781987
1000 genomesrs587781987
hgdprs587781987
ensemblrs587781987
gopubmedrs587781987
geneviewrs587781987
scholarrs587781987
googlers587781987
pharmgkbrs587781987
gwascentralrs587781987
openSNPrs587781987
23andMers587781987
23andMe allrs587781987
SNP Nexus

SNPshotrs587781987
SNPdbers587781987
MSV3drs587781987
GWAS Ctlgrs587781987
Max Magnitude0
ClinVar
Risk rs587781987(;)
Alt rs587781987(;)
Reference rs587781987(TTTGAGGTGC;TTTGAGGTGC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7577121_7577130delGCACCTCAAA
CLNSRC
CLNACC RCV000130388.2,