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rs1057519862

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519862(A;A)
Make rs1057519862(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39723405
GeneERBB2
is asnp
is mentioned by
dbSNPrs1057519862
dbSNP (old)rs1057519862
ClinGenrs1057519862
ebirs1057519862
HLIrs1057519862
Exacrs1057519862
Gnomadrs1057519862
Varsomers1057519862
Maprs1057519862
PheGenIrs1057519862
Biobankrs1057519862
1000 genomesrs1057519862
hgdprs1057519862
ensemblrs1057519862
gopubmedrs1057519862
geneviewrs1057519862
scholarrs1057519862
googlers1057519862
pharmgkbrs1057519862
gwascentralrs1057519862
openSNPrs1057519862
23andMers1057519862
23andMe allrs1057519862
SNPshotrs1057519862
SNPdbers1057519862
MSV3drs1057519862
GWAS Ctlgrs1057519862
Max Magnitude0
ClinVar
Risk rs1057519862(A;A)
Alt rs1057519862(A;A)
Reference Rs1057519862(G;G)
Significance Probable-Pathogenic
Disease Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Neoplasm of breast Adenocarcinoma of prostate Colorectal Neoplasms Adenocarcinoma of stomach
Variation info
Gene ERBB2
CLNDBN Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Neoplasm of breast Adenocarcinoma of prostate Colorectal Neoplasms Adenocarcinoma of stomach
Reversed 0
HGVS NC_000017.10:g.37879658G>A
CLNSRC
CLNACC RCV000417832.1, RCV000420241.1, RCV000424585.1, RCV000428060.1, RCV000437885.1, RCV000438950.1,