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rs876658854

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658854(A;A)
Make rs876658854(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31330499
GeneNF1
is asnp
is mentioned by
dbSNPrs876658854
ebirs876658854
HLIrs876658854
Exacrs876658854
Varsomers876658854
Maprs876658854
PheGenIrs876658854
hapmaprs876658854
1000 genomesrs876658854
hgdprs876658854
ensemblrs876658854
gopubmedrs876658854
geneviewrs876658854
scholarrs876658854
googlers876658854
pharmgkbrs876658854
gwascentralrs876658854
openSNPrs876658854
23andMers876658854
23andMe allrs876658854
SNP Nexus

SNPshotrs876658854
SNPdbers876658854
MSV3drs876658854
GWAS Ctlgrs876658854
Max Magnitude0
ClinVar
Risk rs876658854(A;A)
Alt rs876658854(A;A)
Reference rs876658854(G;G)
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.29657517G>A
CLNSRC
CLNACC RCV000214123.1,