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rs869025648

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025648(A;G)
Make rs869025648(G;G)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10146587
GeneVHL
is asnp
is mentioned by
dbSNPrs869025648
ebirs869025648
HLIrs869025648
Exacrs869025648
Varsomers869025648
Maprs869025648
PheGenIrs869025648
hapmaprs869025648
1000 genomesrs869025648
hgdprs869025648
ensemblrs869025648
gopubmedrs869025648
geneviewrs869025648
scholarrs869025648
googlers869025648
pharmgkbrs869025648
gwascentralrs869025648
openSNPrs869025648
23andMers869025648
23andMe allrs869025648
SNP Nexus

SNPshotrs869025648
SNPdbers869025648
MSV3drs869025648
GWAS Ctlgrs869025648
Max Magnitude0
ClinVar
Risk rs869025648(G;G)
Alt rs869025648(G;G)
Reference rs869025648(A;A)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.10188271A>G
CLNSRC
CLNACC RCV000208865.1, RCV000216698.1,