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rs1064793878

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Chromosome3
Position10149874
GeneVHL
is asnp
is mentioned by
dbSNPrs1064793878
dbSNP (old)rs1064793878
ClinGenrs1064793878
ebirs1064793878
HLIrs1064793878
Exacrs1064793878
Gnomadrs1064793878
Varsomers1064793878
LitVarrs1064793878
Maprs1064793878
PheGenIrs1064793878
Biobankrs1064793878
1000 genomesrs1064793878
hgdprs1064793878
ensemblrs1064793878
gopubmedrs1064793878
geneviewrs1064793878
scholarrs1064793878
googlers1064793878
pharmgkbrs1064793878
gwascentralrs1064793878
openSNPrs1064793878
23andMers1064793878
23andMe allrs1064793878
SNPshotrs1064793878
SNPdbers1064793878
MSV3drs1064793878
GWAS Ctlgrs1064793878
Max Magnitude0
ClinVar
Risk rs1064793878(C;C)
Alt rs1064793878(C;C)
Reference Rs1064793878(T;T)
Significance Pathogenic
Disease not provided
Variation info
Gene VHL
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.10191558T>C
CLNSRC
CLNACC RCV000484822.1,