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rs864622109

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs864622109(C;T)
Make rs864622109(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome3
Position10149878
GeneVHL
is asnp
is mentioned by
dbSNPrs864622109
ebirs864622109
HLIrs864622109
Exacrs864622109
Varsomers864622109
Maprs864622109
PheGenIrs864622109
hapmaprs864622109
1000 genomesrs864622109
hgdprs864622109
ensemblrs864622109
gopubmedrs864622109
geneviewrs864622109
scholarrs864622109
googlers864622109
pharmgkbrs864622109
gwascentralrs864622109
openSNPrs864622109
23andMers864622109
23andMe allrs864622109
SNP Nexus

SNPshotrs864622109
SNPdbers864622109
MSV3drs864622109
GWAS Ctlgrs864622109
Max Magnitude0
ClinVar
Risk rs864622109(T;T)
Alt rs864622109(T;T)
Reference rs864622109(C;C)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000003.11:g.10191562C>G; NC_000003.11:g.10191562C>T
CLNSRC
CLNACC RCV000208826.1, RCV000219064.1, RCV000205143.1,