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rs1064794272

From SNPedia
Orientationplus
Stabilizedplus
Geno Mag Summary
(C;C) 0 common in clinvar
Chromosome3
Position10146566
GeneVHL
is asnp
is mentioned by
dbSNPrs1064794272
dbSNP (old)rs1064794272
ClinGenrs1064794272
ebirs1064794272
HLIrs1064794272
Exacrs1064794272
Gnomadrs1064794272
Varsomers1064794272
Maprs1064794272
PheGenIrs1064794272
Biobankrs1064794272
1000 genomesrs1064794272
hgdprs1064794272
ensemblrs1064794272
gopubmedrs1064794272
geneviewrs1064794272
scholarrs1064794272
googlers1064794272
pharmgkbrs1064794272
gwascentralrs1064794272
openSNPrs1064794272
23andMers1064794272
23andMe allrs1064794272
SNPshotrs1064794272
SNPdbers1064794272
MSV3drs1064794272
GWAS Ctlgrs1064794272
Max Magnitude0
ClinVar
Risk rs1064794272(A;A)
Alt rs1064794272(A;A)
Reference Rs1064794272(C;C)
Significance Probable-Pathogenic
Disease not provided
Variation info
Gene VHL
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.10188250C>A
CLNSRC
CLNACC RCV000482784.1,