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

rs1057519892

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs1057519892(A;T)
Make rs1057519892(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome12
Position56088558
GeneERBB3
is asnp
is mentioned by
dbSNPrs1057519892
dbSNP (classic)rs1057519892
ClinGenrs1057519892
ebirs1057519892
HLIrs1057519892
Exacrs1057519892
Gnomadrs1057519892
Varsomers1057519892
LitVarrs1057519892
Maprs1057519892
PheGenIrs1057519892
Biobankrs1057519892
1000 genomesrs1057519892
hgdprs1057519892
ensemblrs1057519892
geneviewrs1057519892
scholarrs1057519892
googlers1057519892
pharmgkbrs1057519892
gwascentralrs1057519892
openSNPrs1057519892
23andMers1057519892
SNPshotrs1057519892
SNPdbers1057519892
MSV3drs1057519892
GWAS Ctlgrs1057519892
Max Magnitude0
ClinVar
Risk rs1057519892(T;T)
Alt rs1057519892(T;T)
Reference Rs1057519892(A;A)
Significance Probable-Pathogenic
Disease Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Neoplasm of breast Uterine Carcinosarcoma Malignant neoplasm of body of uterus
Variation info
Gene ERBB3
CLNDBN Transitional cell carcinoma of the bladder Adenocarcinoma of stomach Neoplasm of breast Uterine Carcinosarcoma Malignant neoplasm of body of uterus
Reversed 0
HGVS NC_000012.11:g.56482342A>T
CLNSRC
CLNACC RCV000427382.1, RCV000434468.1, RCV000435426.1, RCV000441987.1, RCV000442973.1,