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rs876658541

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876658541(C;T)
Make rs876658541(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31338092
GeneNF1
is asnp
is mentioned by
dbSNPrs876658541
ebirs876658541
HLIrs876658541
Exacrs876658541
Varsomers876658541
Maprs876658541
PheGenIrs876658541
hapmaprs876658541
1000 genomesrs876658541
hgdprs876658541
ensemblrs876658541
gopubmedrs876658541
geneviewrs876658541
scholarrs876658541
googlers876658541
pharmgkbrs876658541
gwascentralrs876658541
openSNPrs876658541
23andMers876658541
23andMe allrs876658541
SNP Nexus

SNPshotrs876658541
SNPdbers876658541
MSV3drs876658541
GWAS Ctlgrs876658541
Max Magnitude0
ClinVar
Risk rs876658541(T;T)
Alt rs876658541(T;T)
Reference rs876658541(C;C)
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.29665110C>T
CLNSRC
CLNACC RCV000223234.1,