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rs876658570

From SNPedia

Orientationplus
Geno Mag Summary
(T;T) 0 common in clinvar
Make rs876658570(G;G)
Make rs876658570(G;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31181464
GeneNF1
is asnp
is mentioned by
dbSNPrs876658570
ebirs876658570
HLIrs876658570
Exacrs876658570
Varsomers876658570
Maprs876658570
PheGenIrs876658570
hapmaprs876658570
1000 genomesrs876658570
hgdprs876658570
ensemblrs876658570
gopubmedrs876658570
geneviewrs876658570
scholarrs876658570
googlers876658570
pharmgkbrs876658570
gwascentralrs876658570
openSNPrs876658570
23andMers876658570
23andMe allrs876658570
SNP Nexus

SNPshotrs876658570
SNPdbers876658570
MSV3drs876658570
GWAS Ctlgrs876658570
Max Magnitude0
ClinVar
Risk rs876658570(G;G)
Alt rs876658570(G;G)
Reference rs876658570(T;T)
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.29508482T>G
CLNSRC
CLNACC RCV000217256.1,