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rs397516444

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs397516444(G;T)
Make rs397516444(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position10149808
GeneVHL
is asnp
is mentioned by
dbSNPrs397516444
ebirs397516444
HLIrs397516444
Exacrs397516444
Varsomers397516444
Maprs397516444
PheGenIrs397516444
hapmaprs397516444
1000 genomesrs397516444
hgdprs397516444
ensemblrs397516444
gopubmedrs397516444
geneviewrs397516444
scholarrs397516444
googlers397516444
pharmgkbrs397516444
gwascentralrs397516444
openSNPrs397516444
23andMers397516444
23andMe allrs397516444
SNP Nexus

SNPshotrs397516444
SNPdbers397516444
MSV3drs397516444
GWAS Ctlgrs397516444
Max Magnitude0
ClinVar
Risk rs397516444(T;T)
Alt rs397516444(T;T)
Reference rs397516444(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.10191492G>A; NC_000003.11:g.10191492G>T
CLNSRC ClinVar
CLNACC RCV000208789.1, RCV000036548.3,