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rs876660782

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660782(G;T)
Make rs876660782(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31201410
GeneNF1
is asnp
is mentioned by
dbSNPrs876660782
ebirs876660782
HLIrs876660782
Exacrs876660782
Varsomers876660782
Maprs876660782
PheGenIrs876660782
hapmaprs876660782
1000 genomesrs876660782
hgdprs876660782
ensemblrs876660782
gopubmedrs876660782
geneviewrs876660782
scholarrs876660782
googlers876660782
pharmgkbrs876660782
gwascentralrs876660782
openSNPrs876660782
23andMers876660782
23andMe allrs876660782
SNP Nexus

SNPshotrs876660782
SNPdbers876660782
MSV3drs876660782
GWAS Ctlgrs876660782
Max Magnitude0
ClinVar
Risk rs876660782(T;T)
Alt rs876660782(T;T)
Reference rs876660782(G;G)
Significance Probable-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.29528428G>T
CLNSRC
CLNACC RCV000217434.1,