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rs866445127

From SNPedia

Orientationplus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs866445127(C;T)
Make rs866445127(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31352348
GeneNF1
is asnp
is mentioned by
dbSNPrs866445127
ebirs866445127
HLIrs866445127
Exacrs866445127
Varsomers866445127
Maprs866445127
PheGenIrs866445127
hapmaprs866445127
1000 genomesrs866445127
hgdprs866445127
ensemblrs866445127
gopubmedrs866445127
geneviewrs866445127
scholarrs866445127
googlers866445127
pharmgkbrs866445127
gwascentralrs866445127
openSNPrs866445127
23andMers866445127
23andMe allrs866445127
SNP Nexus

SNPshotrs866445127
SNPdbers866445127
MSV3drs866445127
GWAS Ctlgrs866445127
Max Magnitude0
ClinVar
Risk rs866445127(T;T)
Alt rs866445127(T;T)
Reference rs866445127(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.29679366C>T
CLNSRC
CLNACC RCV000218957.1,