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rs876660696

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660696(A;A)
Make rs876660696(A;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31335016
GeneNF1
is asnp
is mentioned by
dbSNPrs876660696
ebirs876660696
HLIrs876660696
Exacrs876660696
Varsomers876660696
Maprs876660696
PheGenIrs876660696
hapmaprs876660696
1000 genomesrs876660696
hgdprs876660696
ensemblrs876660696
gopubmedrs876660696
geneviewrs876660696
scholarrs876660696
googlers876660696
pharmgkbrs876660696
gwascentralrs876660696
openSNPrs876660696
23andMers876660696
23andMe allrs876660696
SNP Nexus

SNPshotrs876660696
SNPdbers876660696
MSV3drs876660696
GWAS Ctlgrs876660696
Max Magnitude0
ClinVar
Risk rs876660696(A;A)
Alt rs876660696(A;A)
Reference rs876660696(G;G)
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.29662034G>A
CLNSRC
CLNACC RCV000215669.1,