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rs1642742

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs1642742(C;T)
Make rs1642742(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position10150259
GeneVHL
is asnp
is mentioned by
dbSNPrs1642742
dbSNP (old)rs1642742
ClinGenrs1642742
ebirs1642742
HLIrs1642742
Exacrs1642742
Gnomadrs1642742
Varsomers1642742
Maprs1642742
PheGenIrs1642742
Biobankrs1642742
1000 genomesrs1642742
hgdprs1642742
ensemblrs1642742
gopubmedrs1642742
geneviewrs1642742
scholarrs1642742
googlers1642742
pharmgkbrs1642742
gwascentralrs1642742
openSNPrs1642742
23andMers1642742
23andMe allrs1642742
SNP Nexus

SNPshotrs1642742
SNPdbers1642742
MSV3drs1642742
GWAS Ctlgrs1642742
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 25217002OA-icon.png] Two single nucleotide polymorphisms in the von Hippel-Lindau tumor suppressor gene in Taiwanese with renal cell carcinoma


ClinVar
Risk rs1642742(T;T)
Alt rs1642742(T;T)
Reference Rs1642742(C;C)
Significance Non-pathogenic
Disease Von Hippel-Lindau syndrome
Variation info
Gene VHL
CLNDBN Von Hippel-Lindau syndrome
Reversed 1
HGVS NC_000003.11:g.10191943G>A
CLNSRC
CLNACC RCV000348075.1,