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rs876660135

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs876660135(-;-)
Make rs876660135(-;G)
ReferenceGRCh38.p2 38.2/147
Chromosome17
Position31221922
GeneNF1
is asnp
is mentioned by
dbSNPrs876660135
ebirs876660135
HLIrs876660135
Exacrs876660135
Varsomers876660135
Maprs876660135
PheGenIrs876660135
hapmaprs876660135
1000 genomesrs876660135
hgdprs876660135
ensemblrs876660135
gopubmedrs876660135
geneviewrs876660135
scholarrs876660135
googlers876660135
pharmgkbrs876660135
gwascentralrs876660135
openSNPrs876660135
23andMers876660135
23andMe allrs876660135
SNP Nexus

SNPshotrs876660135
SNPdbers876660135
MSV3drs876660135
GWAS Ctlgrs876660135
Max Magnitude0
ClinVar
Risk rs876660135(;)
Alt rs876660135(;)
Reference rs876660135(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.29548940delG
CLNSRC
CLNACC RCV000221288.1,