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

rs121913468

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913468(C;C)
Make rs121913468(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39724008
GeneERBB2
is asnp
is mentioned by
dbSNPrs121913468
dbSNP (old)rs121913468
ClinGenrs121913468
ebirs121913468
HLIrs121913468
Exacrs121913468
Gnomadrs121913468
Varsomers121913468
Maprs121913468
PheGenIrs121913468
Biobankrs121913468
1000 genomesrs121913468
hgdprs121913468
ensemblrs121913468
gopubmedrs121913468
geneviewrs121913468
scholarrs121913468
googlers121913468
pharmgkbrs121913468
gwascentralrs121913468
openSNPrs121913468
23andMers121913468
23andMe allrs121913468
SNPshotrs121913468
SNPdbers121913468
MSV3drs121913468
GWAS Ctlgrs121913468
Max Magnitude0
ClinVar
Risk rs121913468(A;A) rs121913468(C;C) rs121913468(T;T)
Alt rs121913468(A;A) rs121913468(C;C) rs121913468(T;T)
Reference Rs121913468(G;G)
Significance Pathogenic
Disease Oesophageal carcinoma Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Neoplasm of breast Uterine cervical neoplasms
Variation info
Gene ERBB2
CLNDBN Oesophageal carcinoma Adenocarcinoma of stomach Transitional cell carcinoma of the bladder Neoplasm of breast Uterine cervical neoplasms
Reversed 0
HGVS NC_000017.10:g.37880261G>A; NC_000017.10:g.37880261G>C; NC_000017.10:g.37880261G>T
CLNSRC
CLNACC RCV000419212.1, RCV000420244.1, RCV000430490.1, RCV000431162.1, RCV000441427.1, RCV000423455.1, RCV000426351.1, RCV000433752.1, RCV000444643.1, RCV000445220.1, RCV000418272.1, RCV000427352.1, RCV000437580.1, RCV000438329.1, RCV000443774.1,