rs1057519919

Orientation

plus

Stabilized

plus

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

Make rs1057519919(C;T)

Make rs1057519919(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

15942195

Gene	MYCN, MYCNOS

is a	snp
is	mentioned by
dbSNP	rs1057519919
dbSNP (classic)	rs1057519919
ClinGen	rs1057519919
ebi	rs1057519919
HLI	rs1057519919
Exac	rs1057519919
Gnomad	rs1057519919
Varsome	rs1057519919
LitVar	rs1057519919
Map	rs1057519919
PheGenI	rs1057519919
Biobank	rs1057519919
1000 genomes	rs1057519919
hgdp	rs1057519919
ensembl	rs1057519919
geneview	rs1057519919
scholar	rs1057519919
google	rs1057519919
pharmgkb	rs1057519919
gwascentral	rs1057519919
openSNP	rs1057519919
23andMe	rs1057519919
SNPshot	rs1057519919
SNPdbe	rs1057519919
MSV3d	rs1057519919
GWAS Ctlg	rs1057519919

Max Magnitude

0

ClinVar
Risk	rs1057519919(T;T)
Alt	rs1057519919(T;T)
Reference	Rs1057519919(C;C)
Significance	Probable-Pathogenic
Disease	Malignant neoplasm of body of uterus Glioblastoma Pancreatic adenocarcinoma Neuroblastoma Medulloblastoma
Variation	info
Gene	MYCN MYCNOS
CLNDBN	Malignant neoplasm of body of uterus Glioblastoma Pancreatic adenocarcinoma Neuroblastoma Medulloblastoma
Reversed	0
HGVS	NC_000002.11:g.16082317C>T
CLNSRC
CLNACC	RCV000421370.1, RCV000423772.1, RCV000428589.1, RCV000434477.1, RCV000441008.1,