rs28933407

Orientation

plus

Stabilized

plus

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

Make rs28933407(C;T)

Make rs28933407(T;T)

Reference

GRCh38 38.1/141

Chromosome

8

Position

127738431

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs28933407
dbSNP (classic)	rs28933407
ClinGen	rs28933407
ebi	rs28933407
HLI	rs28933407
Exac	rs28933407
Gnomad	rs28933407
Varsome	rs28933407
LitVar	rs28933407
Map	rs28933407
PheGenI	rs28933407
Biobank	rs28933407
1000 genomes	rs28933407
hgdp	rs28933407
ensembl	rs28933407
geneview	rs28933407
scholar	rs28933407
google	rs28933407
pharmgkb	rs28933407
gwascentral	rs28933407
openSNP	rs28933407
23andMe	rs28933407
SNPshot	rs28933407
SNPdbe	rs28933407
MSV3d	rs28933407
GWAS Ctlg	rs28933407

Max Magnitude

0

OMIM	190080
Desc	BURKITT LYMPHOMA
Variant	0001
Related	also

ClinVar
Risk	rs28933407(T;T)
Alt	rs28933407(T;T)
Reference	Rs28933407(C;C)
Significance	Pathogenic
Disease	Burkitt lymphoma
Variation	info
Gene	MYC
CLNDBN	Burkitt lymphoma
Reversed	0
HGVS	NC_000008.10:g.128750677C>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013402.23,