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rs876658492

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876658492(-;-)
Make rs876658492(-;T)
Make rs876658492(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31265323
GeneNF1
is asnp
is mentioned by
dbSNPrs876658492
ebirs876658492
HLIrs876658492
Exacrs876658492
Varsomers876658492
Maprs876658492
PheGenIrs876658492
hapmaprs876658492
1000 genomesrs876658492
hgdprs876658492
ensemblrs876658492
gopubmedrs876658492
geneviewrs876658492
scholarrs876658492
googlers876658492
pharmgkbrs876658492
gwascentralrs876658492
openSNPrs876658492
23andMers876658492
23andMe allrs876658492
SNP Nexus

SNPshotrs876658492
SNPdbers876658492
MSV3drs876658492
GWAS Ctlgrs876658492
Max Magnitude0
ClinVar
Risk rs876658492(T;T)
Alt rs876658492(T;T)
Reference rs876658492(;)
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.29592341dupT
CLNSRC
CLNACC RCV000215369.1,