Have questions? Visit https://www.reddit.com/r/SNPedia

rs104893824

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs104893824(C;C)
Make rs104893824(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position10142181
GeneVHL
is asnp
is mentioned by
dbSNPrs104893824
ebirs104893824
HLIrs104893824
Exacrs104893824
Varsomers104893824
Maprs104893824
PheGenIrs104893824
hapmaprs104893824
1000 genomesrs104893824
hgdprs104893824
ensemblrs104893824
gopubmedrs104893824
geneviewrs104893824
scholarrs104893824
googlers104893824
pharmgkbrs104893824
gwascentralrs104893824
openSNPrs104893824
23andMers104893824
23andMe allrs104893824
SNP Nexus

SNPshotrs104893824
SNPdbers104893824
MSV3drs104893824
GWAS Ctlgrs104893824
Max Magnitude0
OMIM608537
Desc
Variant0017
Relatedalso
OMIM608537
Desc
Variant0012
Relatedalso
ClinVar
Risk rs104893824(A,C;A,C)
Alt rs104893824(A,C;A,C)
Reference rs104893824(T;T)
Significance Pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 0
HGVS NC_000003.11:g.10183865T>A; NC_000003.11:g.10183865T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002316.3, RCV000002308.2,