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rs869025663

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(TGTCCGGAGCC;TGTCCGGAGCC) 0 common in clinvar
(TGTCCGGAGCCT;TGTCCGGAGCCT) 0 common in clinvar
Make rs869025663(-;-)
Make rs869025663(-;GTCCGGAGCCT)
Make rs869025663(GTCCGGAGCCT;GTCCGGAGCCT)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10149819
GeneVHL
is asnp
is mentioned by
dbSNPrs869025663
dbSNP (old)rs869025663
ClinGenrs869025663
ebirs869025663
HLIrs869025663
Exacrs869025663
Gnomadrs869025663
Varsomers869025663
Maprs869025663
PheGenIrs869025663
Biobankrs869025663
1000 genomesrs869025663
hgdprs869025663
ensemblrs869025663
gopubmedrs869025663
geneviewrs869025663
scholarrs869025663
googlers869025663
pharmgkbrs869025663
gwascentralrs869025663
openSNPrs869025663
23andMers869025663
23andMe allrs869025663
SNP Nexus

SNPshotrs869025663
SNPdbers869025663
MSV3drs869025663
GWAS Ctlgrs869025663
Max Magnitude0
ClinVar
Risk rs869025663(-;-)
Alt rs869025663(-;-)
Reference Rs869025663(TGTCCGGAGCC;TGTCCGGAGCC)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10191503_10191513delGTCCGGAGCCT
CLNSRC
CLNACC RCV000208854.1,