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rs1057519836

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519836(A;C)
Make rs1057519836(C;C)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41224630
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs1057519836
dbSNP (classic)rs1057519836
ClinGenrs1057519836
ebirs1057519836
HLIrs1057519836
Exacrs1057519836
Gnomadrs1057519836
Varsomers1057519836
LitVarrs1057519836
Maprs1057519836
PheGenIrs1057519836
Biobankrs1057519836
1000 genomesrs1057519836
hgdprs1057519836
ensemblrs1057519836
geneviewrs1057519836
scholarrs1057519836
googlers1057519836
pharmgkbrs1057519836
gwascentralrs1057519836
openSNPrs1057519836
23andMers1057519836
23andMe allrs1057519836
SNPshotrs1057519836
SNPdbers1057519836
MSV3drs1057519836
GWAS Ctlgrs1057519836
Max Magnitude0
ClinVar
Risk rs1057519836(C;C) rs1057519836(G;G) rs1057519836(T;T)
Alt rs1057519836(C;C) rs1057519836(G;G) rs1057519836(T;T)
Reference Rs1057519836(A;A)
Significance Probable-Pathogenic
Disease Neoplasm Neoplasm of stomach
Variation info
Gene CTNNB1
CLNDBN Neoplasm Neoplasm of stomach
Reversed 0
HGVS NC_000003.11:g.41266121A>C; NC_000003.11:g.41266121A>G; NC_000003.11:g.41266121A>T
CLNSRC
CLNACC RCV000425513.1, RCV000433725.1, RCV000444185.1,