Have questions? Visit https://www.reddit.com/r/SNPedia

rs876658245

From SNPedia

Orientationplus
Geno Mag Summary
(A;A) 0 common in clinvar
Make rs876658245(-;-)
Make rs876658245(-;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31349164
GeneNF1
is asnp
is mentioned by
dbSNPrs876658245
ebirs876658245
HLIrs876658245
Exacrs876658245
Varsomers876658245
Maprs876658245
PheGenIrs876658245
hapmaprs876658245
1000 genomesrs876658245
hgdprs876658245
ensemblrs876658245
gopubmedrs876658245
geneviewrs876658245
scholarrs876658245
googlers876658245
pharmgkbrs876658245
gwascentralrs876658245
openSNPrs876658245
23andMers876658245
23andMe allrs876658245
SNP Nexus

SNPshotrs876658245
SNPdbers876658245
MSV3drs876658245
GWAS Ctlgrs876658245
Max Magnitude0
ClinVar
Risk rs876658245(;)
Alt rs876658245(;)
Reference rs876658245(A;A)
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.29676182delA
CLNSRC
CLNACC RCV000223023.1,