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rs11575996

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11575996(A;A)
Make rs11575996(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7673535
GeneTP53
is asnp
is mentioned by
dbSNPrs11575996
dbSNP (classic)rs11575996
ClinGenrs11575996
ebirs11575996
HLIrs11575996
Exacrs11575996
Gnomadrs11575996
Varsomers11575996
LitVarrs11575996
Maprs11575996
PheGenIrs11575996
Biobankrs11575996
1000 genomesrs11575996
hgdprs11575996
ensemblrs11575996
geneviewrs11575996
scholarrs11575996
googlers11575996
pharmgkbrs11575996
gwascentralrs11575996
openSNPrs11575996
23andMers11575996
23andMe allrs11575996
SNPshotrs11575996
SNPdbers11575996
MSV3drs11575996
GWAS Ctlgrs11575996
Max Magnitude0
ClinVar
Risk rs11575996(A;A) rs11575996(T;T)
Alt rs11575996(A;A) rs11575996(T;T)
Reference Rs11575996(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000017.10:g.7576853C>T
CLNSRC
CLNACC RCV000492456.1,