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rs876660580

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660580(-;-)
Make rs876660580(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31233019
GeneNF1
is asnp
is mentioned by
dbSNPrs876660580
ebirs876660580
HLIrs876660580
Exacrs876660580
Varsomers876660580
Maprs876660580
PheGenIrs876660580
hapmaprs876660580
1000 genomesrs876660580
hgdprs876660580
ensemblrs876660580
gopubmedrs876660580
geneviewrs876660580
scholarrs876660580
googlers876660580
pharmgkbrs876660580
gwascentralrs876660580
openSNPrs876660580
23andMers876660580
23andMe allrs876660580
SNP Nexus

SNPshotrs876660580
SNPdbers876660580
MSV3drs876660580
GWAS Ctlgrs876660580
Max Magnitude0
ClinVar
Risk rs876660580(;)
Alt rs876660580(;)
Reference rs876660580(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.29560037delG
CLNSRC
CLNACC RCV000219024.1,