Have questions? Visit https://www.reddit.com/r/SNPedia

rs864321640

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(-;-) 0 common in clinvar
Make rs864321640(-;A)
Make rs864321640(A;A)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position10149911
GeneVHL
is asnp
is mentioned by
dbSNPrs864321640
ClinGenrs864321640
ebirs864321640
HLIrs864321640
Exacrs864321640
Varsomers864321640
Maprs864321640
PheGenIrs864321640
hapmaprs864321640
1000 genomesrs864321640
hgdprs864321640
ensemblrs864321640
gopubmedrs864321640
geneviewrs864321640
scholarrs864321640
googlers864321640
pharmgkbrs864321640
gwascentralrs864321640
openSNPrs864321640
23andMers864321640
23andMe allrs864321640
SNP Nexus

SNPshotrs864321640
SNPdbers864321640
MSV3drs864321640
GWAS Ctlgrs864321640
Max Magnitude0
ClinVar
Risk rs864321640(A;A)
Alt rs864321640(A;A)
Reference Rs864321640(-;-)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene VHL
CLNDBN Pheochromocytoma
Reversed 0
HGVS NC_000003.11:g.10191595dupA
CLNSRC Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000203546.1,