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rs1057519891

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519891(G;T)
Make rs1057519891(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position56088557
GeneERBB3
is asnp
is mentioned by
dbSNPrs1057519891
dbSNP (old)rs1057519891
ClinGenrs1057519891
ebirs1057519891
HLIrs1057519891
Exacrs1057519891
Gnomadrs1057519891
Varsomers1057519891
LitVarrs1057519891
Maprs1057519891
PheGenIrs1057519891
Biobankrs1057519891
1000 genomesrs1057519891
hgdprs1057519891
ensemblrs1057519891
gopubmedrs1057519891
geneviewrs1057519891
scholarrs1057519891
googlers1057519891
pharmgkbrs1057519891
gwascentralrs1057519891
openSNPrs1057519891
23andMers1057519891
23andMe allrs1057519891
SNPshotrs1057519891
SNPdbers1057519891
MSV3drs1057519891
GWAS Ctlgrs1057519891
Max Magnitude0
ClinVar
Risk rs1057519891(A;A) rs1057519891(T;T)
Alt rs1057519891(A;A) rs1057519891(T;T)
Reference Rs1057519891(G;G)
Significance Probable-Pathogenic
Disease Uterine Carcinosarcoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Neoplasm of breast
Variation info
Gene ERBB3
CLNDBN Uterine Carcinosarcoma Malignant neoplasm of body of uterus Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Neoplasm of breast
Reversed 0
HGVS NC_000012.11:g.56482341G>A; NC_000012.11:g.56482341G>T
CLNSRC
CLNACC RCV000418815.1, RCV000424484.1, RCV000429499.1, RCV000435185.1, RCV000435793.1, RCV000423102.1, RCV000424195.1, RCV000433369.1, RCV000440744.1, RCV000443967.1,