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rs869025632

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(ACCGAGGTACG;ACCGAGGTACG) 0 common in clinvar
(TACCGAGGTACG;TACCGAGGTACG) 0 common in clinvar
Make rs869025632(-;-)
Make rs869025632(-;ACCGAGGTACG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142182
GeneVHL
is asnp
is mentioned by
dbSNPrs869025632
ClinGenrs869025632
ebirs869025632
HLIrs869025632
Exacrs869025632
Varsomers869025632
Maprs869025632
PheGenIrs869025632
hapmaprs869025632
1000 genomesrs869025632
hgdprs869025632
ensemblrs869025632
gopubmedrs869025632
geneviewrs869025632
scholarrs869025632
googlers869025632
pharmgkbrs869025632
gwascentralrs869025632
openSNPrs869025632
23andMers869025632
23andMe allrs869025632
SNP Nexus

SNPshotrs869025632
SNPdbers869025632
MSV3drs869025632
GWAS Ctlgrs869025632
Max Magnitude0
ClinVar
Risk rs869025632(-;-)
Alt rs869025632(-;-)
Reference Rs869025632(ACCGAGGTACG;ACCGAGGTACG)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183866_10183876delACCGAGGTACG
CLNSRC
CLNACC RCV000208806.1,