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rs1057519890

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519890(A;A)
Make rs1057519890(A;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39723966
GeneERBB2
is asnp
is mentioned by
dbSNPrs1057519890
dbSNP (old)rs1057519890
ClinGenrs1057519890
ebirs1057519890
HLIrs1057519890
Exacrs1057519890
Gnomadrs1057519890
Varsomers1057519890
LitVarrs1057519890
Maprs1057519890
PheGenIrs1057519890
Biobankrs1057519890
1000 genomesrs1057519890
hgdprs1057519890
ensemblrs1057519890
gopubmedrs1057519890
geneviewrs1057519890
scholarrs1057519890
googlers1057519890
pharmgkbrs1057519890
gwascentralrs1057519890
openSNPrs1057519890
23andMers1057519890
23andMe allrs1057519890
SNPshotrs1057519890
SNPdbers1057519890
MSV3drs1057519890
GWAS Ctlgrs1057519890
Max Magnitude0
ClinVar
Risk rs1057519890(A;A)
Alt rs1057519890(A;A)
Reference Rs1057519890(T;T)
Significance Probable-Pathogenic
Disease Papillary renal cell carcinoma Colorectal Neoplasms Neoplasm of breast Malignant melanoma of skin Malignant neoplasm of body of uterus Adenocarcinoma of stomach Transitional cell carcinoma of the bladder
Variation info
Gene ERBB2
CLNDBN Papillary renal cell carcinoma, sporadic Colorectal Neoplasms Neoplasm of breast Malignant melanoma of skin Malignant neoplasm of body of uterus Adenocarcinoma of stomach Transitional cell carcinoma of the bladder
Reversed 0
HGVS NC_000017.10:g.37880219T>A
CLNSRC
CLNACC RCV000421368.1, RCV000422582.1, RCV000431643.1, RCV000432868.1, RCV000438379.1, RCV000439036.1, RCV000443340.1,