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rs876659964

From SNPedia

Orientationplus
Geno Mag Summary
(;) 0 common in clinvar
Make rs876659964(-;-)
Make rs876659964(-;T)
Make rs876659964(T;T)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31258436
GeneNF1
is asnp
is mentioned by
dbSNPrs876659964
ebirs876659964
HLIrs876659964
Exacrs876659964
Varsomers876659964
Maprs876659964
PheGenIrs876659964
hapmaprs876659964
1000 genomesrs876659964
hgdprs876659964
ensemblrs876659964
gopubmedrs876659964
geneviewrs876659964
scholarrs876659964
googlers876659964
pharmgkbrs876659964
gwascentralrs876659964
openSNPrs876659964
23andMers876659964
23andMe allrs876659964
SNP Nexus

SNPshotrs876659964
SNPdbers876659964
MSV3drs876659964
GWAS Ctlgrs876659964
Max Magnitude0
ClinVar
Risk rs876659964(T;T)
Alt rs876659964(T;T)
Reference rs876659964(;)
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.29585454dupT
CLNSRC
CLNACC RCV000218073.1,