rs121918684

Orientation

plus

Stabilized

plus

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

Make rs121918684(C;C)

Make rs121918684(C;G)

Reference

GRCh38 38.1/141

Chromosome

8

Position

127738379

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs121918684
dbSNP (classic)	rs121918684
ClinGen	rs121918684
ebi	rs121918684
HLI	rs121918684
Exac	rs121918684
Gnomad	rs121918684
Varsome	rs121918684
LitVar	rs121918684
Map	rs121918684
PheGenI	rs121918684
Biobank	rs121918684
1000 genomes	rs121918684
hgdp	rs121918684
ensembl	rs121918684
geneview	rs121918684
scholar	rs121918684
google	rs121918684
pharmgkb	rs121918684
gwascentral	rs121918684
openSNP	rs121918684
23andMe	rs121918684
SNPshot	rs121918684
SNPdbe	rs121918684
MSV3d	rs121918684
GWAS Ctlg	rs121918684

Max Magnitude

0

OMIM	190080
Desc
Variant	0003
Related	also

ClinVar
Risk	rs121918684(C;C)
Alt	rs121918684(C;C)
Reference	Rs121918684(G;G)
Significance	Pathogenic
Disease	Burkitt lymphoma
Variation	info
Gene	MYC
CLNDBN	Burkitt lymphoma
Reversed	0
HGVS	NC_000008.10:g.128750625G>C
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000013404.18,