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rs5030802

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs5030802(A;A)
Make rs5030802(A;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position10142055
GeneVHL
is asnp
is mentioned by
dbSNPrs5030802
ebirs5030802
HLIrs5030802
Exacrs5030802
Varsomers5030802
Maprs5030802
PheGenIrs5030802
hapmaprs5030802
1000 genomesrs5030802
hgdprs5030802
ensemblrs5030802
gopubmedrs5030802
geneviewrs5030802
scholarrs5030802
googlers5030802
pharmgkbrs5030802
gwascentralrs5030802
openSNPrs5030802
23andMers5030802
23andMe allrs5030802
SNP Nexus

SNPshotrs5030802
SNPdbers5030802
MSV3drs5030802
GWAS Ctlgrs5030802
Max Magnitude0
ClinVar
Risk rs5030802(A,T;A,T)
Alt rs5030802(A,T;A,T)
Reference rs5030802(G;G)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183739G>A
CLNSRC ClinVar
CLNACC RCV000036540.3,