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rs28940297

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs28940297(C;C)
Make rs28940297(C;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position10149811
GeneVHL
is asnp
is mentioned by
dbSNPrs28940297
ebirs28940297
HLIrs28940297
Exacrs28940297
Varsomers28940297
Maprs28940297
PheGenIrs28940297
hapmaprs28940297
1000 genomesrs28940297
hgdprs28940297
ensemblrs28940297
gopubmedrs28940297
geneviewrs28940297
scholarrs28940297
googlers28940297
pharmgkbrs28940297
gwascentralrs28940297
openSNPrs28940297
23andMers28940297
23andMe allrs28940297
SNP Nexus

SNPshotrs28940297
SNPdbers28940297
MSV3drs28940297
GWAS Ctlgrs28940297
Max Magnitude0
OMIM608537
DescRENAL CELL CARCINOMA WITH PARANEOPLASTIC ERYTHROCYTOSIS
Variant0018
Relatedalso
Neighborrs28940299
Distance245


ClinVar
Risk rs28940297(C;C)
Alt rs28940297(C;C)
Reference rs28940297(T;T)
Significance Pathogenic
Disease Renal cell carcinoma with paraneoplastic erythrocytosis
Variation info
Gene VHL
CLNDBN Renal cell carcinoma with paraneoplastic erythrocytosis
Reversed 0
HGVS NC_000003.11:g.10191495T>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000002319.3,