rs121918685

Orientation

plus

Stabilized

plus

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

Make rs121918685(C;G)

Make rs121918685(G;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

127738437

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs121918685
dbSNP (classic)	rs121918685
ClinGen	rs121918685
ebi	rs121918685
HLI	rs121918685
Exac	rs121918685
Gnomad	rs121918685
Varsome	rs121918685
LitVar	rs121918685
Map	rs121918685
PheGenI	rs121918685
Biobank	rs121918685
1000 genomes	rs121918685
hgdp	rs121918685
ensembl	rs121918685
geneview	rs121918685
scholar	rs121918685
google	rs121918685
pharmgkb	rs121918685
gwascentral	rs121918685
openSNP	rs121918685
23andMe	rs121918685
SNPshot	rs121918685
SNPdbe	rs121918685
MSV3d	rs121918685
GWAS Ctlg	rs121918685

Max Magnitude

0

OMIM	190080
Desc
Variant	0004
Related	also

ClinVar
Risk	rs121918685(G;G)
Alt	rs121918685(G;G)
Reference	Rs121918685(C;C)
Significance	Pathogenic
Disease	Burkitt lymphoma
Variation	info
Gene	MYC
CLNDBN	Burkitt lymphoma
Reversed	0
HGVS	NC_000008.10:g.128750683C>G
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013405.20,