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rs869025634

From SNPedia

Orientationplus
Geno Mag Summary
(GGTAC;GGTAC) 0 common in clinvar
Make rs869025634(-;-)
Make rs869025634(-;TACGG)
Make rs869025634(TACGG;TACGG)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142189
GeneVHL
is asnp
is mentioned by
dbSNPrs869025634
ebirs869025634
HLIrs869025634
Exacrs869025634
Varsomers869025634
Maprs869025634
PheGenIrs869025634
hapmaprs869025634
1000 genomesrs869025634
hgdprs869025634
ensemblrs869025634
gopubmedrs869025634
geneviewrs869025634
scholarrs869025634
googlers869025634
pharmgkbrs869025634
gwascentralrs869025634
openSNPrs869025634
23andMers869025634
23andMe allrs869025634
SNP Nexus

SNPshotrs869025634
SNPdbers869025634
MSV3drs869025634
GWAS Ctlgrs869025634
Max Magnitude0
ClinVar
Risk rs869025634(;)
Alt rs869025634(;)
Reference rs869025634(GGTAC;GGTAC)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183873_10183877delTACGG
CLNSRC
CLNACC RCV000208840.1,