rs1057519849

Orientation

plus

Stabilized

plus

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

Make rs1057519849(C;T)

Make rs1057519849(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

127738386

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs1057519849
dbSNP (classic)	rs1057519849
ClinGen	rs1057519849
ebi	rs1057519849
HLI	rs1057519849
Exac	rs1057519849
Gnomad	rs1057519849
Varsome	rs1057519849
LitVar	rs1057519849
Map	rs1057519849
PheGenI	rs1057519849
Biobank	rs1057519849
1000 genomes	rs1057519849
hgdp	rs1057519849
ensembl	rs1057519849
geneview	rs1057519849
scholar	rs1057519849
google	rs1057519849
pharmgkb	rs1057519849
gwascentral	rs1057519849
openSNP	rs1057519849
23andMe	rs1057519849
SNPshot	rs1057519849
SNPdbe	rs1057519849
MSV3d	rs1057519849
GWAS Ctlg	rs1057519849

Max Magnitude

0

ClinVar
Risk	rs1057519849(T;T)
Alt	rs1057519849(T;T)
Reference	Rs1057519849(C;C)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	MYC
CLNDBN	Neoplasm
Reversed	0
HGVS	NC_000008.10:g.128750632C>T
CLNSRC
CLNACC	RCV000429575.1,