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rs1057519893

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519893(A;A)
Make rs1057519893(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position56085070
GeneERBB3
is asnp
is mentioned by
dbSNPrs1057519893
dbSNP (old)rs1057519893
ClinGenrs1057519893
ebirs1057519893
HLIrs1057519893
Exacrs1057519893
Gnomadrs1057519893
Varsomers1057519893
Maprs1057519893
PheGenIrs1057519893
Biobankrs1057519893
1000 genomesrs1057519893
hgdprs1057519893
ensemblrs1057519893
gopubmedrs1057519893
geneviewrs1057519893
scholarrs1057519893
googlers1057519893
pharmgkbrs1057519893
gwascentralrs1057519893
openSNPrs1057519893
23andMers1057519893
23andMe allrs1057519893
SNPshotrs1057519893
SNPdbers1057519893
MSV3drs1057519893
GWAS Ctlgrs1057519893
Max Magnitude0
ClinVar
Risk rs1057519893(A;A) rs1057519893(T;T)
Alt rs1057519893(A;A) rs1057519893(T;T)
Reference Rs1057519893(G;G)
Significance Probable-Pathogenic
Disease Adenocarcinoma of stomach Uterine Carcinosarcoma Uterine cervical neoplasms Neoplasm of breast Colorectal Neoplasms Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Carcinoma of gallbladder
Variation info
Gene ERBB3
CLNDBN Adenocarcinoma of stomach Uterine Carcinosarcoma Uterine cervical neoplasms Neoplasm of breast Colorectal Neoplasms Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Carcinoma of gallbladder
Reversed 0
HGVS NC_000012.11:g.56478854G>A; NC_000012.11:g.56478854G>T
CLNSRC
CLNACC RCV000418579.1, RCV000422734.1, RCV000424151.1, RCV000429939.1, RCV000430165.1, RCV000434002.1, RCV000440793.1, RCV000441492.1, RCV000421354.1, RCV000424621.1, RCV000425620.1, RCV000432050.1, RCV000436217.1, RCV000443475.1, RCV000443618.1, RCV000443705.1,