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rs864321642

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs864321642(C;C)
Make rs864321642(C;T)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position10149832
GeneVHL
is asnp
is mentioned by
dbSNPrs864321642
ebirs864321642
HLIrs864321642
Exacrs864321642
Varsomers864321642
Maprs864321642
PheGenIrs864321642
hapmaprs864321642
1000 genomesrs864321642
hgdprs864321642
ensemblrs864321642
gopubmedrs864321642
geneviewrs864321642
scholarrs864321642
googlers864321642
pharmgkbrs864321642
gwascentralrs864321642
openSNPrs864321642
23andMers864321642
23andMe allrs864321642
SNP Nexus

SNPshotrs864321642
SNPdbers864321642
MSV3drs864321642
GWAS Ctlgrs864321642
Max Magnitude0
ClinVar
Risk rs864321642(C;C)
Alt rs864321642(C;C)
Reference rs864321642(T;T)
Significance Probable-Pathogenic
Disease Pheochromocytoma
Variation info
Gene VHL
CLNDBN Pheochromocytoma
Reversed 0
HGVS NC_000003.11:g.10191516T>C
CLNSRC Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000203560.1,