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rs864321643

From SNPedia

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Geno Mag Summary
(A;A) 0 common in clinvar
Make rs864321643(A;C)
Make rs864321643(C;C)
ReferenceGRCh38.p2 38.2/146
Chromosome3
Position10142140
GeneVHL
is asnp
is mentioned by
dbSNPrs864321643
ebirs864321643
HLIrs864321643
Exacrs864321643
Varsomers864321643
Maprs864321643
PheGenIrs864321643
hapmaprs864321643
1000 genomesrs864321643
hgdprs864321643
ensemblrs864321643
gopubmedrs864321643
geneviewrs864321643
scholarrs864321643
googlers864321643
pharmgkbrs864321643
gwascentralrs864321643
openSNPrs864321643
23andMers864321643
23andMe allrs864321643
SNP Nexus

SNPshotrs864321643
SNPdbers864321643
MSV3drs864321643
GWAS Ctlgrs864321643
Max Magnitude0
ClinVar
Risk rs864321643(C;C)
Alt rs864321643(C;C)
Reference rs864321643(A;A)
Significance Pathogenic
Disease Pheochromocytoma Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Pheochromocytoma Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183824A>C; NC_000003.11:g.10183824A>G
CLNSRC Seth G.S. Medical College and K.E.M. Hospital
CLNACC RCV000203508.1, RCV000208847.1, RCV000208825.1,