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rs876660444

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs876660444(C;T)
Make rs876660444(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31229871
GeneNF1
is asnp
is mentioned by
dbSNPrs876660444
ebirs876660444
HLIrs876660444
Exacrs876660444
Varsomers876660444
Maprs876660444
PheGenIrs876660444
hapmaprs876660444
1000 genomesrs876660444
hgdprs876660444
ensemblrs876660444
gopubmedrs876660444
geneviewrs876660444
scholarrs876660444
googlers876660444
pharmgkbrs876660444
gwascentralrs876660444
openSNPrs876660444
23andMers876660444
23andMe allrs876660444
SNP Nexus

SNPshotrs876660444
SNPdbers876660444
MSV3drs876660444
GWAS Ctlgrs876660444
Max Magnitude0
ClinVar
Risk rs876660444(T;T)
Alt rs876660444(T;T)
Reference rs876660444(C;C)
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.29556889C>T
CLNSRC
CLNACC RCV000219051.1,