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rs876660826

From SNPedia

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Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660826(G;G)
Make rs876660826(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31227608
GeneNF1
is asnp
is mentioned by
dbSNPrs876660826
ebirs876660826
HLIrs876660826
Exacrs876660826
Varsomers876660826
Maprs876660826
PheGenIrs876660826
hapmaprs876660826
1000 genomesrs876660826
hgdprs876660826
ensemblrs876660826
gopubmedrs876660826
geneviewrs876660826
scholarrs876660826
googlers876660826
pharmgkbrs876660826
gwascentralrs876660826
openSNPrs876660826
23andMers876660826
23andMe allrs876660826
SNP Nexus

SNPshotrs876660826
SNPdbers876660826
MSV3drs876660826
GWAS Ctlgrs876660826
Max Magnitude0
ClinVar
Risk rs876660826(G;G)
Alt rs876660826(G;G)
Reference rs876660826(T;T)
Significance Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene NF1
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 0
HGVS NC_000017.10:g.29554626T>G
CLNSRC
CLNACC RCV000213190.1,