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

rs587780096

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs587780096(C;C)
Make rs587780096(C;G)
ReferenceGRCh38.p7 38.3/150
Chromosome8
Position89980889
GeneNBN
is asnp
is mentioned by
dbSNPrs587780096
dbSNP (classic)rs587780096
ClinGenrs587780096
ebirs587780096
HLIrs587780096
Exacrs587780096
Gnomadrs587780096
Varsomers587780096
LitVarrs587780096
Maprs587780096
PheGenIrs587780096
Biobankrs587780096
1000 genomesrs587780096
hgdprs587780096
ensemblrs587780096
geneviewrs587780096
scholarrs587780096
googlers587780096
pharmgkbrs587780096
gwascentralrs587780096
openSNPrs587780096
23andMers587780096
23andMe allrs587780096
SNPshotrs587780096
SNPdbers587780096
MSV3drs587780096
GWAS Ctlgrs587780096
Max Magnitude0
ClinVar
Risk rs587780096(C;C) rs587780096(T;T)
Alt rs587780096(C;C) rs587780096(T;T)
Reference Rs587780096(G;G)
Significance Pathogenic
Disease not provided not specified
Variation info
Gene NBN
CLNDBN not provided not specified
Reversed 1
HGVS NC_000008.10:g.90993117C>A; NC_000008.10:g.90993117C>G
CLNSRC
CLNACC RCV000485413.1, RCV000115793.2,