rs775522201

Orientation

plus

Stabilized

plus

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

Make rs775522201(C;T)

Make rs775522201(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

127738393

Gene

MYC

is a	snp
is	mentioned by
dbSNP	rs775522201
dbSNP (classic)	rs775522201
ClinGen	rs775522201
ebi	rs775522201
HLI	rs775522201
Exac	rs775522201
Gnomad	rs775522201
Varsome	rs775522201
LitVar	rs775522201
Map	rs775522201
PheGenI	rs775522201
Biobank	rs775522201
1000 genomes	rs775522201
hgdp	rs775522201
ensembl	rs775522201
geneview	rs775522201
scholar	rs775522201
google	rs775522201
pharmgkb	rs775522201
gwascentral	rs775522201
openSNP	rs775522201
23andMe	rs775522201
SNPshot	rs775522201
SNPdbe	rs775522201
MSV3d	rs775522201
GWAS Ctlg	rs775522201

Max Magnitude

0

ClinVar
Risk	rs775522201(T;T)
Alt	rs775522201(T;T)
Reference	Rs775522201(C;C)
Significance	Probable-Pathogenic
Disease	Neoplasm
Variation	info
Gene	MYC
CLNDBN	Neoplasm
Reversed	0
HGVS	NC_000008.10:g.128750639C>T
CLNSRC
CLNACC	RCV000440255.1,