Have questions? Visit https://www.reddit.com/r/SNPedia

rs876659666

From SNPedia

Orientationminus
Geno Mag Summary
(GTCTGTTTT;GTCTGTTTT) 0 common in clinvar
Make rs876659666(ACA;ACA)
Make rs876659666(ACA;GTCTGTTTT)
ReferenceGRCh38.p2 38.2/147
Chromosome8
Position89955274
GeneNBN
is asnp
is mentioned by
dbSNPrs876659666
ebirs876659666
HLIrs876659666
Exacrs876659666
Varsomers876659666
Maprs876659666
PheGenIrs876659666
hapmaprs876659666
1000 genomesrs876659666
hgdprs876659666
ensemblrs876659666
gopubmedrs876659666
geneviewrs876659666
scholarrs876659666
googlers876659666
pharmgkbrs876659666
gwascentralrs876659666
openSNPrs876659666
23andMers876659666
23andMe allrs876659666
SNP Nexus

SNPshotrs876659666
SNPdbers876659666
MSV3drs876659666
GWAS Ctlgrs876659666
Max Magnitude0
ClinVar
Risk rs876659666(ACA;ACA)
Alt rs876659666(ACA;ACA)
Reference rs876659666(GTCTGTTTT;GTCTGTTTT)
Significance Probable-Pathogenic
Disease Tumor susceptibility linked to germline BAP1 mutations
Variation info
Gene NBN
CLNDBN Tumor susceptibility linked to germline BAP1 mutations
Reversed 1
HGVS NC_000008.10:g.90967502_90967510delAAAACAGACinsTGT
CLNSRC
CLNACC RCV000214006.1,