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rs876660212

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660212(-;-)
Make rs876660212(-;T)
Make rs876660212(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31330416
GeneNF1
is asnp
is mentioned by
dbSNPrs876660212
ebirs876660212
HLIrs876660212
Exacrs876660212
Varsomers876660212
Maprs876660212
PheGenIrs876660212
hapmaprs876660212
1000 genomesrs876660212
hgdprs876660212
ensemblrs876660212
gopubmedrs876660212
geneviewrs876660212
scholarrs876660212
googlers876660212
pharmgkbrs876660212
gwascentralrs876660212
openSNPrs876660212
23andMers876660212
23andMe allrs876660212
SNP Nexus

SNPshotrs876660212
SNPdbers876660212
MSV3drs876660212
GWAS Ctlgrs876660212
Max Magnitude0
ClinVar
Risk rs876660212(T;T)
Alt rs876660212(T;T)
Reference rs876660212(;)
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.29657434dupT
CLNSRC
CLNACC RCV000214983.1,