rs1057519851

Orientation

plus

Stabilized

plus

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

Make rs1057519851(C;G)

Make rs1057519851(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

127738995

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs1057519851
dbSNP (classic)	rs1057519851
ClinGen	rs1057519851
ebi	rs1057519851
HLI	rs1057519851
Exac	rs1057519851
Gnomad	rs1057519851
Varsome	rs1057519851
LitVar	rs1057519851
Map	rs1057519851
PheGenI	rs1057519851
Biobank	rs1057519851
1000 genomes	rs1057519851
hgdp	rs1057519851
ensembl	rs1057519851
geneview	rs1057519851
scholar	rs1057519851
google	rs1057519851
pharmgkb	rs1057519851
gwascentral	rs1057519851
openSNP	rs1057519851
23andMe	rs1057519851
SNPshot	rs1057519851
SNPdbe	rs1057519851
MSV3d	rs1057519851
GWAS Ctlg	rs1057519851

Max Magnitude

0

ClinVar
Risk	rs1057519851(G;G)
Alt	rs1057519851(G;G)
Reference	Rs1057519851(C;C)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	MYC
CLNDBN	Neoplasm
Reversed	0
HGVS	NC_000008.10:g.128751241C>G
CLNSRC
CLNACC	RCV000444724.1,