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rs121913471

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs121913471(G;T)
Make rs121913471(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39724747
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs121913471
dbSNP (old)rs121913471
ClinGenrs121913471
ebirs121913471
HLIrs121913471
Exacrs121913471
Gnomadrs121913471
Varsomers121913471
Maprs121913471
PheGenIrs121913471
Biobankrs121913471
1000 genomesrs121913471
hgdprs121913471
ensemblrs121913471
gopubmedrs121913471
geneviewrs121913471
scholarrs121913471
googlers121913471
pharmgkbrs121913471
gwascentralrs121913471
openSNPrs121913471
23andMers121913471
23andMe allrs121913471
SNPshotrs121913471
SNPdbers121913471
MSV3drs121913471
GWAS Ctlgrs121913471
Max Magnitude0
ClinVar
Risk rs121913471(A;A) rs121913471(C;C) rs121913471(T;T)
Alt rs121913471(A;A) rs121913471(C;C) rs121913471(T;T)
Reference Rs121913471(G;G)
Significance Pathogenic
Disease Adenocarcinoma of stomach Colorectal Neoplasms Neoplasm of breast not specified
Variation info
Gene ERBB2 MIR4728
CLNDBN Adenocarcinoma of stomach Colorectal Neoplasms Neoplasm of breast not specified
Reversed 0
HGVS NC_000017.10:g.37881000G>A; NC_000017.10:g.37881000G>C; NC_000017.10:g.37881000G>T
CLNSRC
CLNACC RCV000422009.1, RCV000428744.1, RCV000439665.1, RCV000439788.1, RCV000038130.2, RCV000417571.1, RCV000428506.1, RCV000435242.1,