rs1057519890

Orientation

plus

Stabilized

plus

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

Make rs1057519890(A;A)

Make rs1057519890(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

17

Position

39723966

Gene

ERBB2

is a	snp
is	mentioned by
dbSNP	rs1057519890
dbSNP (classic)	rs1057519890
ClinGen	rs1057519890
ebi	rs1057519890
HLI	rs1057519890
Exac	rs1057519890
Gnomad	rs1057519890
Varsome	rs1057519890
LitVar	rs1057519890
Map	rs1057519890
PheGenI	rs1057519890
Biobank	rs1057519890
1000 genomes	rs1057519890
hgdp	rs1057519890
ensembl	rs1057519890
geneview	rs1057519890
scholar	rs1057519890
google	rs1057519890
pharmgkb	rs1057519890
gwascentral	rs1057519890
openSNP	rs1057519890
23andMe	rs1057519890
SNPshot	rs1057519890
SNPdbe	rs1057519890
MSV3d	rs1057519890
GWAS Ctlg	rs1057519890

Max Magnitude

0

ClinVar
Risk	rs1057519890(A;A)
Alt	rs1057519890(A;A)
Reference	Rs1057519890(T;T)
Significance	Probable-Pathogenic
Disease	Papillary renal cell carcinoma Colorectal Neoplasms Neoplasm of breast Malignant melanoma of skin Malignant neoplasm of body of uterus Adenocarcinoma of stomach Transitional cell carcinoma of the bladder
Variation	info
Gene	ERBB2
CLNDBN	Papillary renal cell carcinoma, sporadic Colorectal Neoplasms Neoplasm of breast Malignant melanoma of skin Malignant neoplasm of body of uterus Adenocarcinoma of stomach Transitional cell carcinoma of the bladder
Reversed	0
HGVS	NC_000017.10:g.37880219T>A
CLNSRC
CLNACC	RCV000421368.1, RCV000422582.1, RCV000431643.1, RCV000432868.1, RCV000438379.1, RCV000439036.1, RCV000443340.1,