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rs876658235

From SNPedia

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Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876658235(A;A)
Make rs876658235(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31235988
GeneNF1
is asnp
is mentioned by
dbSNPrs876658235
ebirs876658235
HLIrs876658235
Exacrs876658235
Varsomers876658235
Maprs876658235
PheGenIrs876658235
hapmaprs876658235
1000 genomesrs876658235
hgdprs876658235
ensemblrs876658235
gopubmedrs876658235
geneviewrs876658235
scholarrs876658235
googlers876658235
pharmgkbrs876658235
gwascentralrs876658235
openSNPrs876658235
23andMers876658235
23andMe allrs876658235
SNP Nexus

SNPshotrs876658235
SNPdbers876658235
MSV3drs876658235
GWAS Ctlgrs876658235
Max Magnitude0
ClinVar
Risk rs876658235(A;A)
Alt rs876658235(A;A)
Reference rs876658235(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.29563006G>A
CLNSRC
CLNACC RCV000213654.1,