rs121918683

Orientation

plus

Stabilized

plus

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

Make rs121918683(A;C)

Make rs121918683(C;C)

Reference

GRCh38 38.1/141

Chromosome

8

Position

127738519

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs121918683
dbSNP (classic)	rs121918683
ClinGen	rs121918683
ebi	rs121918683
HLI	rs121918683
Exac	rs121918683
Gnomad	rs121918683
Varsome	rs121918683
LitVar	rs121918683
Map	rs121918683
PheGenI	rs121918683
Biobank	rs121918683
1000 genomes	rs121918683
hgdp	rs121918683
ensembl	rs121918683
geneview	rs121918683
scholar	rs121918683
google	rs121918683
pharmgkb	rs121918683
gwascentral	rs121918683
openSNP	rs121918683
23andMe	rs121918683
SNPshot	rs121918683
SNPdbe	rs121918683
MSV3d	rs121918683
GWAS Ctlg	rs121918683

Max Magnitude

0

OMIM	190080
Desc
Variant	0002
Related	also

ClinVar
Risk	rs121918683(C;C)
Alt	rs121918683(C;C)
Reference	Rs121918683(A;A)
Significance	Pathogenic
Disease	Burkitt lymphoma Neoplasm
Variation	info
Gene	MYC
CLNDBN	Burkitt lymphoma Neoplasm
Reversed	0
HGVS	NC_000008.10:g.128750765A>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013403.20, RCV000431563.1,