rs1057519918

Orientation

plus

Stabilized

plus

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

Make rs1057519918(C;T)

Make rs1057519918(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

127738390

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs1057519918
dbSNP (classic)	rs1057519918
ClinGen	rs1057519918
ebi	rs1057519918
HLI	rs1057519918
Exac	rs1057519918
Gnomad	rs1057519918
Varsome	rs1057519918
LitVar	rs1057519918
Map	rs1057519918
PheGenI	rs1057519918
Biobank	rs1057519918
1000 genomes	rs1057519918
hgdp	rs1057519918
ensembl	rs1057519918
geneview	rs1057519918
scholar	rs1057519918
google	rs1057519918
pharmgkb	rs1057519918
gwascentral	rs1057519918
openSNP	rs1057519918
23andMe	rs1057519918
SNPshot	rs1057519918
SNPdbe	rs1057519918
MSV3d	rs1057519918
GWAS Ctlg	rs1057519918

Max Magnitude

0

ClinVar
Risk	rs1057519918(T;T)
Alt	rs1057519918(T;T)
Reference	Rs1057519918(C;C)
Significance	Probable-Pathogenic
Disease	Malignant lymphoma Adenocarcinoma of lung Oesophageal carcinoma Neuroblastoma Malignant melanoma of skin
Variation	info
Gene	MYC
CLNDBN	Malignant lymphoma, non-Hodgkin Adenocarcinoma of lung Oesophageal carcinoma Neuroblastoma Malignant melanoma of skin
Reversed	0
HGVS	NC_000008.10:g.128750636C>T
CLNSRC
CLNACC	RCV000418915.1, RCV000427867.1, RCV000428982.1, RCV000436178.1, RCV000438593.1,