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

rs11575997

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs11575997(C;C)
Make rs11575997(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position7673534
GeneTP53
is asnp
is mentioned by
dbSNPrs11575997
dbSNP (old)rs11575997
ClinGenrs11575997
ebirs11575997
HLIrs11575997
Exacrs11575997
Gnomadrs11575997
Varsomers11575997
LitVarrs11575997
Maprs11575997
PheGenIrs11575997
Biobankrs11575997
1000 genomesrs11575997
hgdprs11575997
ensemblrs11575997
gopubmedrs11575997
geneviewrs11575997
scholarrs11575997
googlers11575997
pharmgkbrs11575997
gwascentralrs11575997
openSNPrs11575997
23andMers11575997
23andMe allrs11575997
SNPshotrs11575997
SNPdbers11575997
MSV3drs11575997
GWAS Ctlgrs11575997
Max Magnitude0
ClinVar
Risk rs11575997(C;C) rs11575997(T;T)
Alt rs11575997(C;C) rs11575997(T;T)
Reference Rs11575997(G;G)
Significance Pathogenic
Disease not provided
Variation info
Gene TP53
CLNDBN not provided
Reversed 1
HGVS NC_000017.10:g.7576852C>G
CLNSRC
CLNACC RCV000429174.1,