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rs4902359

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs4902359(A;A)
Make rs4902359(A;G)
ReferenceGRCh38 38.1/141
Chromosome14
Position65076072
GeneMAX
is asnp
is mentioned by
dbSNPrs4902359
dbSNP (old)rs4902359
ClinGenrs4902359
ebirs4902359
HLIrs4902359
Exacrs4902359
Gnomadrs4902359
Varsomers4902359
Maprs4902359
PheGenIrs4902359
Biobankrs4902359
1000 genomesrs4902359
hgdprs4902359
ensemblrs4902359
gopubmedrs4902359
geneviewrs4902359
scholarrs4902359
googlers4902359
pharmgkbrs4902359
gwascentralrs4902359
openSNPrs4902359
23andMers4902359
23andMe allrs4902359
SNP Nexus

SNPshotrs4902359
SNPdbers4902359
MSV3drs4902359
GWAS Ctlgrs4902359
GMAF0.4596
Max Magnitude0
? (A;A) (A;G) (G;G) 28
[PMID 23743562] MAX mutations status in Swedish patients with pheochromocytoma and paraganglioma tumours


ClinVar
Risk rs4902359(A;A)
Alt rs4902359(A;A)
Reference Rs4902359(G;G)
Significance Non-pathogenic
Disease Pheochromocytoma
Variation info
Gene MAX
CLNDBN Pheochromocytoma
Reversed 0
HGVS NC_000014.8:g.65542790G>A
CLNSRC
CLNACC RCV000325472.1,