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rs775522201

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs775522201(C;T)
Make rs775522201(T;T)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position127738393
GeneMYC
is asnp
is mentioned by
dbSNPrs775522201
dbSNP (classic)rs775522201
ClinGenrs775522201
ebirs775522201
HLIrs775522201
Exacrs775522201
Gnomadrs775522201
Varsomers775522201
LitVarrs775522201
Maprs775522201
PheGenIrs775522201
Biobankrs775522201
1000 genomesrs775522201
hgdprs775522201
ensemblrs775522201
geneviewrs775522201
scholarrs775522201
googlers775522201
pharmgkbrs775522201
gwascentralrs775522201
openSNPrs775522201
23andMers775522201
SNPshotrs775522201
SNPdbers775522201
MSV3drs775522201
GWAS Ctlgrs775522201
Max Magnitude0
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,