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rs869025661

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs869025661(-;-)
Make rs869025661(-;T)
Make rs869025661(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10149794
GeneVHL
is asnp
is mentioned by
dbSNPrs869025661
ebirs869025661
HLIrs869025661
Exacrs869025661
Varsomers869025661
Maprs869025661
PheGenIrs869025661
hapmaprs869025661
1000 genomesrs869025661
hgdprs869025661
ensemblrs869025661
gopubmedrs869025661
geneviewrs869025661
scholarrs869025661
googlers869025661
pharmgkbrs869025661
gwascentralrs869025661
openSNPrs869025661
23andMers869025661
23andMe allrs869025661
SNP Nexus

SNPshotrs869025661
SNPdbers869025661
MSV3drs869025661
GWAS Ctlgrs869025661
Max Magnitude0
ClinVar
Risk rs869025661(T;T)
Alt rs869025661(T;T)
Reference rs869025661(;)
Significance Probable-Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10191478dupT
CLNSRC
CLNACC RCV000208814.1,