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rs869025621

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs869025621(A;T)
Make rs869025621(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10142079
GeneVHL
is asnp
is mentioned by
dbSNPrs869025621
ebirs869025621
HLIrs869025621
Exacrs869025621
Varsomers869025621
Maprs869025621
PheGenIrs869025621
hapmaprs869025621
1000 genomesrs869025621
hgdprs869025621
ensemblrs869025621
gopubmedrs869025621
geneviewrs869025621
scholarrs869025621
googlers869025621
pharmgkbrs869025621
gwascentralrs869025621
openSNPrs869025621
23andMers869025621
23andMe allrs869025621
SNP Nexus

SNPshotrs869025621
SNPdbers869025621
MSV3drs869025621
GWAS Ctlgrs869025621
Max Magnitude0
ClinVar
Risk rs869025621(T;T)
Alt rs869025621(T;T)
Reference rs869025621(A;A)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183763A>T
CLNSRC
CLNACC RCV000208818.1,