rs1057519893

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs1057519893(A;A)

Make rs1057519893(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

12

Position

56085070

Gene

ERBB3

is a	snp
is	mentioned by
dbSNP	rs1057519893
dbSNP (classic)	rs1057519893
ClinGen	rs1057519893
ebi	rs1057519893
HLI	rs1057519893
Exac	rs1057519893
Gnomad	rs1057519893
Varsome	rs1057519893
LitVar	rs1057519893
Map	rs1057519893
PheGenI	rs1057519893
Biobank	rs1057519893
1000 genomes	rs1057519893
hgdp	rs1057519893
ensembl	rs1057519893
geneview	rs1057519893
scholar	rs1057519893
google	rs1057519893
pharmgkb	rs1057519893
gwascentral	rs1057519893
openSNP	rs1057519893
23andMe	rs1057519893
SNPshot	rs1057519893
SNPdbe	rs1057519893
MSV3d	rs1057519893
GWAS Ctlg	rs1057519893

Max Magnitude

0

ClinVar
Risk	rs1057519893(A;A) rs1057519893(T;T)
Alt	rs1057519893(A;A) rs1057519893(T;T)
Reference	Rs1057519893(G;G)
Significance	Probable-Pathogenic
Disease	Adenocarcinoma of stomach Uterine Carcinosarcoma Uterine cervical neoplasms Neoplasm of breast Colorectal Neoplasms Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Carcinoma of gallbladder
Variation	info
Gene	ERBB3
CLNDBN	Adenocarcinoma of stomach Uterine Carcinosarcoma Uterine cervical neoplasms Neoplasm of breast Colorectal Neoplasms Malignant neoplasm of body of uterus Transitional cell carcinoma of the bladder Carcinoma of gallbladder
Reversed	0
HGVS	NC_000012.11:g.56478854G>A; NC_000012.11:g.56478854G>T
CLNSRC
CLNACC	RCV000418579.1, RCV000422734.1, RCV000424151.1, RCV000429939.1, RCV000430165.1, RCV000434002.1, RCV000440793.1, RCV000441492.1, RCV000421354.1, RCV000424621.1, RCV000425620.1, RCV000432050.1, RCV000436217.1, RCV000443475.1, RCV000443618.1, RCV000443705.1,