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rs1064794037

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(GCGAT;GCGAT) 0 common in clinvar
Chromosome3
Position10149805
GeneVHL
is asnp
is mentioned by
dbSNPrs1064794037
dbSNP (old)rs1064794037
ClinGenrs1064794037
ebirs1064794037
HLIrs1064794037
Exacrs1064794037
Gnomadrs1064794037
Varsomers1064794037
Maprs1064794037
PheGenIrs1064794037
Biobankrs1064794037
1000 genomesrs1064794037
hgdprs1064794037
ensemblrs1064794037
gopubmedrs1064794037
geneviewrs1064794037
scholarrs1064794037
googlers1064794037
pharmgkbrs1064794037
gwascentralrs1064794037
openSNPrs1064794037
23andMers1064794037
23andMe allrs1064794037
SNPshotrs1064794037
SNPdbers1064794037
MSV3drs1064794037
GWAS Ctlgrs1064794037
Max Magnitude0
ClinVar
Risk rs1064794037(-;-)
Alt rs1064794037(-;-)
Reference Rs1064794037(GCGAT;GCGAT)
Significance Pathogenic
Disease not provided
Variation info
Gene VHL
CLNDBN not provided
Reversed 0
HGVS NC_000003.11:g.10191489_10191493delGATGC
CLNSRC
CLNACC RCV000480482.1,