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rs1057519857

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs1057519857(C;C)
Make rs1057519857(C;T)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39724772
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs1057519857
dbSNP (old)rs1057519857
ClinGenrs1057519857
ebirs1057519857
HLIrs1057519857
Exacrs1057519857
Gnomadrs1057519857
Varsomers1057519857
Maprs1057519857
PheGenIrs1057519857
Biobankrs1057519857
1000 genomesrs1057519857
hgdprs1057519857
ensemblrs1057519857
gopubmedrs1057519857
geneviewrs1057519857
scholarrs1057519857
googlers1057519857
pharmgkbrs1057519857
gwascentralrs1057519857
openSNPrs1057519857
23andMers1057519857
23andMe allrs1057519857
SNPshotrs1057519857
SNPdbers1057519857
MSV3drs1057519857
GWAS Ctlgrs1057519857
Max Magnitude0
ClinVar
Risk rs1057519857(C;C)
Alt rs1057519857(C;C)
Reference Rs1057519857(T;T)
Significance Probable-Pathogenic
Disease Neoplasm of breast
Variation info
Gene ERBB2 MIR4728
CLNDBN Neoplasm of breast
Reversed 0
HGVS NC_000017.10:g.37881025T>C
CLNSRC
CLNACC RCV000442075.1,