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rs876659471

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659471(-;-)
Make rs876659471(-;T)
Make rs876659471(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31336793
GeneNF1
is asnp
is mentioned by
dbSNPrs876659471
ebirs876659471
HLIrs876659471
Exacrs876659471
Varsomers876659471
Maprs876659471
PheGenIrs876659471
hapmaprs876659471
1000 genomesrs876659471
hgdprs876659471
ensemblrs876659471
gopubmedrs876659471
geneviewrs876659471
scholarrs876659471
googlers876659471
pharmgkbrs876659471
gwascentralrs876659471
openSNPrs876659471
23andMers876659471
23andMe allrs876659471
SNP Nexus

SNPshotrs876659471
SNPdbers876659471
MSV3drs876659471
GWAS Ctlgrs876659471
Max Magnitude0
ClinVar
Risk rs876659471(T;T)
Alt rs876659471(T;T)
Reference rs876659471(;)
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.29663811_29663812insT
CLNSRC
CLNACC RCV000219829.1,