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rs768378152

From SNPedia

Orientationplus
Geno Mag Summary
(TC;TC) 0 common in clinvar
Make rs768378152(-;-)
Make rs768378152(-;TC)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position89981513
GeneNBN
is asnp
is mentioned by
dbSNPrs768378152
ebirs768378152
HLIrs768378152
Exacrs768378152
Varsomers768378152
Maprs768378152
PheGenIrs768378152
hapmaprs768378152
1000 genomesrs768378152
hgdprs768378152
ensemblrs768378152
gopubmedrs768378152
geneviewrs768378152
scholarrs768378152
googlers768378152
pharmgkbrs768378152
gwascentralrs768378152
openSNPrs768378152
23andMers768378152
23andMe allrs768378152
SNP Nexus

SNPshotrs768378152
SNPdbers768378152
MSV3drs768378152
GWAS Ctlgrs768378152
Max Magnitude0
ClinVar
Risk rs768378152(;)
Alt rs768378152(;)
Reference rs768378152(TC;TC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 0
HGVS NC_000008.10:g.90993741_90993742delTC
CLNSRC
CLNACC RCV000166151.1,