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rs876658658

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658658(C;T)
Make rs876658658(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31095340
GeneLOC105371722, MIR4733, NF1
is asnp
is mentioned by
dbSNPrs876658658
ebirs876658658
HLIrs876658658
Exacrs876658658
Varsomers876658658
Maprs876658658
PheGenIrs876658658
hapmaprs876658658
1000 genomesrs876658658
hgdprs876658658
ensemblrs876658658
gopubmedrs876658658
geneviewrs876658658
scholarrs876658658
googlers876658658
pharmgkbrs876658658
gwascentralrs876658658
openSNPrs876658658
23andMers876658658
23andMe allrs876658658
SNP Nexus

SNPshotrs876658658
SNPdbers876658658
MSV3drs876658658
GWAS Ctlgrs876658658
Max Magnitude0
ClinVar
Risk rs876658658(T;T)
Alt rs876658658(T;T)
Reference rs876658658(C;C)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations not provided
Variation info
Gene NF1 MIR4733
CLNDBN Tumor susceptibility linked to germline BAP1 mutations not provided
Reversed 0
HGVS NC_000017.10:g.29422358C>T
CLNSRC
CLNACC RCV000216917.1, RCV000222237.1,