rs750664148

Orientation

plus

Stabilized

plus

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

Make rs750664148(A;C)

Make rs750664148(C;C)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

127738434

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs750664148
dbSNP (classic)	rs750664148
ClinGen	rs750664148
ebi	rs750664148
HLI	rs750664148
Exac	rs750664148
Gnomad	rs750664148
Varsome	rs750664148
LitVar	rs750664148
Map	rs750664148
PheGenI	rs750664148
Biobank	rs750664148
1000 genomes	rs750664148
hgdp	rs750664148
ensembl	rs750664148
geneview	rs750664148
scholar	rs750664148
google	rs750664148
pharmgkb	rs750664148
gwascentral	rs750664148
openSNP	rs750664148
23andMe	rs750664148
SNPshot	rs750664148
SNPdbe	rs750664148
MSV3d	rs750664148
GWAS Ctlg	rs750664148

Max Magnitude

0

ClinVar
Risk	rs750664148(C;C)
Alt	rs750664148(C;C)
Reference	Rs750664148(A;A)
Significance	Probable-Pathogenic
Disease	Neuroblastoma Malignant lymphoma Malignant melanoma of skin Oesophageal carcinoma Adenocarcinoma of lung
Variation	info
Gene	MYC
CLNDBN	Neuroblastoma Malignant lymphoma, non-Hodgkin Malignant melanoma of skin Oesophageal carcinoma Adenocarcinoma of lung
Reversed	0
HGVS	NC_000008.10:g.128750680A>C
CLNSRC
CLNACC	RCV000420006.1, RCV000426528.1, RCV000437207.1, RCV000438328.1, RCV000445053.1,