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rs121913470

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs121913470(C;C)
Make rs121913470(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39723967
GeneERBB2
is asnp
is mentioned by
dbSNPrs121913470
dbSNP (classic)rs121913470
ClinGenrs121913470
ebirs121913470
HLIrs121913470
Exacrs121913470
Gnomadrs121913470
Varsomers121913470
LitVarrs121913470
Maprs121913470
PheGenIrs121913470
Biobankrs121913470
1000 genomesrs121913470
hgdprs121913470
ensemblrs121913470
geneviewrs121913470
scholarrs121913470
googlers121913470
pharmgkbrs121913470
gwascentralrs121913470
openSNPrs121913470
23andMers121913470
23andMe allrs121913470
SNPshotrs121913470
SNPdbers121913470
MSV3drs121913470
GWAS Ctlgrs121913470
Max Magnitude0
ClinVar
Risk rs121913470(C;C) rs121913470(G;G)
Alt rs121913470(C;C) rs121913470(G;G)
Reference Rs121913470(T;T)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Papillary renal cell carcinoma Colorectal Neoplasms Malignant melanoma of skin Transitional cell carcinoma of the bladder Neoplasm of breast Adenocarcinoma of stomach
Variation info
Gene ERBB2
CLNDBN Malignant neoplasm of body of uterus Papillary renal cell carcinoma, sporadic Colorectal Neoplasms Malignant melanoma of skin Transitional cell carcinoma of the bladder Neoplasm of breast Adenocarcinoma of stomach
Reversed 0
HGVS NC_000017.10:g.37880220T>C; NC_000017.10:g.37880220T>G
CLNSRC
CLNACC RCV000417433.1, RCV000418445.1, RCV000427447.1, RCV000428572.1, RCV000429126.1, RCV000435086.1, RCV000435324.1, RCV000417866.1, RCV000425422.1, RCV000426066.1, RCV000432853.1, RCV000435694.1, RCV000442700.1, RCV000445218.1,