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rs876660099

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876660099(A;A)
Make rs876660099(A;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31206278
GeneNF1
is asnp
is mentioned by
dbSNPrs876660099
ebirs876660099
HLIrs876660099
Exacrs876660099
Varsomers876660099
Maprs876660099
PheGenIrs876660099
hapmaprs876660099
1000 genomesrs876660099
hgdprs876660099
ensemblrs876660099
gopubmedrs876660099
geneviewrs876660099
scholarrs876660099
googlers876660099
pharmgkbrs876660099
gwascentralrs876660099
openSNPrs876660099
23andMers876660099
23andMe allrs876660099
SNP Nexus

SNPshotrs876660099
SNPdbers876660099
MSV3drs876660099
GWAS Ctlgrs876660099
Max Magnitude0
ClinVar
Risk rs876660099(A;A)
Alt rs876660099(A;A)
Reference rs876660099(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.29533296T>A
CLNSRC
CLNACC RCV000219851.1,