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rs876660141

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660141(A;A)
Make rs876660141(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31327498
GeneNF1
is asnp
is mentioned by
dbSNPrs876660141
ebirs876660141
HLIrs876660141
Exacrs876660141
Varsomers876660141
Maprs876660141
PheGenIrs876660141
hapmaprs876660141
1000 genomesrs876660141
hgdprs876660141
ensemblrs876660141
gopubmedrs876660141
geneviewrs876660141
scholarrs876660141
googlers876660141
pharmgkbrs876660141
gwascentralrs876660141
openSNPrs876660141
23andMers876660141
23andMe allrs876660141
SNP Nexus

SNPshotrs876660141
SNPdbers876660141
MSV3drs876660141
GWAS Ctlgrs876660141
Max Magnitude0
ClinVar
Risk rs876660141(A;A)
Alt rs876660141(A;A)
Reference rs876660141(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.29654516G>A
CLNSRC
CLNACC RCV000219734.1,