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rs1057519837

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1057519837(C;G)
Make rs1057519837(G;G)
ReferenceGRCh38.p7 38.3/150
Chromosome3
Position41224631
GeneCTNNB1
is asnp
is mentioned by
dbSNPrs1057519837
dbSNP (old)rs1057519837
ClinGenrs1057519837
ebirs1057519837
HLIrs1057519837
Exacrs1057519837
Gnomadrs1057519837
Varsomers1057519837
Maprs1057519837
PheGenIrs1057519837
Biobankrs1057519837
1000 genomesrs1057519837
hgdprs1057519837
ensemblrs1057519837
gopubmedrs1057519837
geneviewrs1057519837
scholarrs1057519837
googlers1057519837
pharmgkbrs1057519837
gwascentralrs1057519837
openSNPrs1057519837
23andMers1057519837
23andMe allrs1057519837
SNPshotrs1057519837
SNPdbers1057519837
MSV3drs1057519837
GWAS Ctlgrs1057519837
Max Magnitude0
ClinVar
Risk rs1057519837(G;G) rs1057519837(T;T)
Alt rs1057519837(G;G) rs1057519837(T;T)
Reference Rs1057519837(C;C)
Significance Probable-Pathogenic
Disease Neoplasm Malignant melanoma
Variation info
Gene CTNNB1
CLNDBN Neoplasm Malignant melanoma
Reversed 0
HGVS NC_000003.11:g.41266122C>G; NC_000003.11:g.41266122C>T
CLNSRC
CLNACC RCV000426279.1, RCV000436951.1,