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

rs786203180

From SNPedia

Orientationminus
Geno Mag Summary
(CC;CC) 0 common in clinvar
Make rs786203180(A;A)
Make rs786203180(A;CC)
ReferenceGRCh38.p2 38.2/146
Chromosome8
Position89953605
GeneNBN
is asnp
is mentioned by
dbSNPrs786203180
ebirs786203180
HLIrs786203180
Exacrs786203180
Varsomers786203180
Maprs786203180
PheGenIrs786203180
hapmaprs786203180
1000 genomesrs786203180
hgdprs786203180
ensemblrs786203180
gopubmedrs786203180
geneviewrs786203180
scholarrs786203180
googlers786203180
pharmgkbrs786203180
gwascentralrs786203180
openSNPrs786203180
23andMers786203180
23andMe allrs786203180
SNP Nexus

SNPshotrs786203180
SNPdbers786203180
MSV3drs786203180
GWAS Ctlgrs786203180
Max Magnitude0
ClinVar
Risk rs786203180(A;A)
Alt rs786203180(A;A)
Reference rs786203180(CC;CC)
Significance Pathogenic
Disease Hereditary cancer-predisposing syndrome
Variation info
Gene NBN
CLNDBN Hereditary cancer-predisposing syndrome
Reversed 1
HGVS NC_000008.10:g.90965833_90965834delGGinsT
CLNSRC
CLNACC RCV000166379.1,