rs1057519962

Orientation

plus

Stabilized

plus

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

Make rs1057519962(A;A)

Make rs1057519962(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

18

Position

51067035

Gene

SMAD4

is a	snp
is	mentioned by
dbSNP	rs1057519962
dbSNP (classic)	rs1057519962
ClinGen	rs1057519962
ebi	rs1057519962
HLI	rs1057519962
Exac	rs1057519962
Gnomad	rs1057519962
Varsome	rs1057519962
LitVar	rs1057519962
Map	rs1057519962
PheGenI	rs1057519962
Biobank	rs1057519962
1000 genomes	rs1057519962
hgdp	rs1057519962
ensembl	rs1057519962
geneview	rs1057519962
scholar	rs1057519962
google	rs1057519962
pharmgkb	rs1057519962
gwascentral	rs1057519962
openSNP	rs1057519962
23andMe	rs1057519962
SNPshot	rs1057519962
SNPdbe	rs1057519962
MSV3d	rs1057519962
GWAS Ctlg	rs1057519962

Max Magnitude

0

ClinVar
Risk	rs1057519962(A;A) rs1057519962(T;T)
Alt	rs1057519962(A;A) rs1057519962(T;T)
Reference	Rs1057519962(G;G)
Significance	Probable-Pathogenic
Disease	Oesophageal carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Adenocarcinoma of stomach Adenocarcinoma of prostate
Variation	info
Gene	SMAD4
CLNDBN	Oesophageal carcinoma Adenocarcinoma of lung Pancreatic adenocarcinoma Colorectal Neoplasms Adenocarcinoma of stomach Adenocarcinoma of prostate
Reversed	0
HGVS	NC_000018.9:g.48593405G>A; NC_000018.9:g.48593405G>T
CLNSRC
CLNACC	RCV000419978.1, RCV000421895.1, RCV000429536.1, RCV000430240.1, RCV000439617.1, RCV000439753.1, RCV000421325.1, RCV000421536.1, RCV000431585.1, RCV000434360.1, RCV000439155.1, RCV000444559.1,