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

rs149633775

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs149633775(A;A)
Make rs149633775(A;G)
ReferenceGRCh38 38.1/142
Chromosome17
Position7673773
GeneTP53
is asnp
is mentioned by
dbSNPrs149633775
ebirs149633775
HLIrs149633775
Exacrs149633775
Varsomers149633775
Maprs149633775
PheGenIrs149633775
hapmaprs149633775
1000 genomesrs149633775
hgdprs149633775
ensemblrs149633775
gopubmedrs149633775
geneviewrs149633775
scholarrs149633775
googlers149633775
pharmgkbrs149633775
gwascentralrs149633775
openSNPrs149633775
23andMers149633775
23andMe allrs149633775
SNP Nexus

SNPshotrs149633775
SNPdbers149633775
MSV3drs149633775
GWAS Ctlgrs149633775
Max Magnitude0
ClinVar
Risk rs149633775(A,T;A,T)
Alt rs149633775(A,T;A,T)
Reference rs149633775(G;G)
Significance Probable-Pathogenic
Disease Hereditary cancer-predisposing syndrome not specified Neoplasm of stomach Li-Fraumeni syndrome Li-Fraumeni syndrome 1
Variation info
Gene TP53
CLNDBN Hereditary cancer-predisposing syndrome not specified Neoplasm of stomach Li-Fraumeni syndrome Li-Fraumeni syndrome 1
Reversed 0
HGVS NC_000017.10:g.7577091G>A
CLNSRC Ambry Genetics ClinVar GeneDx University of Washington
CLNACC RCV000115739.5, RCV000122178.1, RCV000148912.1, RCV000200641.3, RCV000238755.1,