rs1057519850

Orientation

plus

Stabilized

plus

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

Make rs1057519850(C;T)

Make rs1057519850(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

127738447

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs1057519850
dbSNP (classic)	rs1057519850
ClinGen	rs1057519850
ebi	rs1057519850
HLI	rs1057519850
Exac	rs1057519850
Gnomad	rs1057519850
Varsome	rs1057519850
LitVar	rs1057519850
Map	rs1057519850
PheGenI	rs1057519850
Biobank	rs1057519850
1000 genomes	rs1057519850
hgdp	rs1057519850
ensembl	rs1057519850
geneview	rs1057519850
scholar	rs1057519850
google	rs1057519850
pharmgkb	rs1057519850
gwascentral	rs1057519850
openSNP	rs1057519850
23andMe	rs1057519850
SNPshot	rs1057519850
SNPdbe	rs1057519850
MSV3d	rs1057519850
GWAS Ctlg	rs1057519850

Max Magnitude

0

ClinVar
Risk	rs1057519850(T;T)
Alt	rs1057519850(T;T)
Reference	Rs1057519850(C;C)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	MYC
CLNDBN	Neoplasm
Reversed	0
HGVS	NC_000008.10:g.128750693C>T
CLNSRC
CLNACC	RCV000424357.1,