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rs876660286

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs876660286(-;-)
Make rs876660286(-;TC)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31326007
GeneNF1
is asnp
is mentioned by
dbSNPrs876660286
ebirs876660286
HLIrs876660286
Exacrs876660286
Varsomers876660286
Maprs876660286
PheGenIrs876660286
hapmaprs876660286
1000 genomesrs876660286
hgdprs876660286
ensemblrs876660286
gopubmedrs876660286
geneviewrs876660286
scholarrs876660286
googlers876660286
pharmgkbrs876660286
gwascentralrs876660286
openSNPrs876660286
23andMers876660286
23andMe allrs876660286
SNP Nexus

SNPshotrs876660286
SNPdbers876660286
MSV3drs876660286
GWAS Ctlgrs876660286
Max Magnitude0
ClinVar
Risk rs876660286(;)
Alt rs876660286(;)
Reference rs876660286(TC;TC)
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.29653025_29653026delTC
CLNSRC
CLNACC RCV000214739.1,