rs756091827

Orientation

plus

Stabilized

plus

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

Make rs756091827(C;T)

Make rs756091827(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

127738435

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs756091827
dbSNP (classic)	rs756091827
ClinGen	rs756091827
ebi	rs756091827
HLI	rs756091827
Exac	rs756091827
Gnomad	rs756091827
Varsome	rs756091827
LitVar	rs756091827
Map	rs756091827
PheGenI	rs756091827
Biobank	rs756091827
1000 genomes	rs756091827
hgdp	rs756091827
ensembl	rs756091827
geneview	rs756091827
scholar	rs756091827
google	rs756091827
pharmgkb	rs756091827
gwascentral	rs756091827
openSNP	rs756091827
23andMe	rs756091827
SNPshot	rs756091827
SNPdbe	rs756091827
MSV3d	rs756091827
GWAS Ctlg	rs756091827

Max Magnitude

0

ClinVar
Risk	rs756091827(G;G) rs756091827(T;T)
Alt	rs756091827(G;G) rs756091827(T;T)
Reference	Rs756091827(C;C)
Significance	Probable-Pathogenic
Disease	Malignant lymphoma Neoplasm Adenocarcinoma of lung Oesophageal carcinoma Malignant melanoma of skin Neuroblastoma
Variation	info
Gene	MYC
CLNDBN	Malignant lymphoma, non-Hodgkin Neoplasm Adenocarcinoma of lung Oesophageal carcinoma Malignant melanoma of skin Neuroblastoma
Reversed	0
HGVS	NC_000008.10:g.128750681C>T
CLNSRC
CLNACC	RCV000419562.1, RCV000423713.1, RCV000430246.1, RCV000434207.1, RCV000440950.1, RCV000441422.1,