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rs876660931

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876660931(-;-)
Make rs876660931(-;A)
Make rs876660931(A;A)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31200488
GeneNF1
is asnp
is mentioned by
dbSNPrs876660931
ebirs876660931
HLIrs876660931
Exacrs876660931
Varsomers876660931
Maprs876660931
PheGenIrs876660931
hapmaprs876660931
1000 genomesrs876660931
hgdprs876660931
ensemblrs876660931
gopubmedrs876660931
geneviewrs876660931
scholarrs876660931
googlers876660931
pharmgkbrs876660931
gwascentralrs876660931
openSNPrs876660931
23andMers876660931
23andMe allrs876660931
SNP Nexus

SNPshotrs876660931
SNPdbers876660931
MSV3drs876660931
GWAS Ctlgrs876660931
Max Magnitude0
ClinVar
Risk rs876660931(A;A)
Alt rs876660931(A;A)
Reference rs876660931(;)
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.29527506dupA
CLNSRC
CLNACC RCV000219150.1,