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rs1057519738

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs1057519738(A;A)
Make rs1057519738(A;G)
ReferenceGRCh38.p7 38.3/150
Chromosome17
Position39725079
GeneERBB2, MIR4728
is asnp
is mentioned by
dbSNPrs1057519738
dbSNP (old)rs1057519738
ClinGenrs1057519738
ebirs1057519738
HLIrs1057519738
Exacrs1057519738
Gnomadrs1057519738
Varsomers1057519738
Maprs1057519738
PheGenIrs1057519738
Biobankrs1057519738
1000 genomesrs1057519738
hgdprs1057519738
ensemblrs1057519738
gopubmedrs1057519738
geneviewrs1057519738
scholarrs1057519738
googlers1057519738
pharmgkbrs1057519738
gwascentralrs1057519738
openSNPrs1057519738
23andMers1057519738
23andMe allrs1057519738
SNPshotrs1057519738
SNPdbers1057519738
MSV3drs1057519738
GWAS Ctlgrs1057519738
Max Magnitude0
ClinVar
Risk rs1057519738(A;A)
Alt rs1057519738(A;A)
Reference Rs1057519738(G;G)
Significance Pathogenic
Disease Uterine Carcinosarcoma Neoplasm of breast Malignant neoplasm of body of uterus Carcinoma of gallbladder Colorectal Neoplasms Adenocarcinoma of stomach Pancreatic adenocarcinoma
Variation info
Gene ERBB2 MIR4728
CLNDBN Uterine Carcinosarcoma Neoplasm of breast Malignant neoplasm of body of uterus Carcinoma of gallbladder Colorectal Neoplasms Adenocarcinoma of stomach Pancreatic adenocarcinoma
Reversed 0
HGVS NC_000017.10:g.37881332G>A
CLNSRC
CLNACC RCV000422021.1, RCV000423067.1, RCV000428793.1, RCV000433354.1, RCV000439690.1, RCV000440770.1, RCV000444555.1,