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rs767215758

From SNPedia

Orientationplus
Geno Mag Summary
(G;G) 0 common in clinvar
Make rs767215758(A;A)
Make rs767215758(A;G)
ReferenceGRCh38.p2 38.2/144
Chromosome8
Position89958819
GeneNBN
is asnp
is mentioned by
dbSNPrs767215758
ebirs767215758
HLIrs767215758
Exacrs767215758
Varsomers767215758
Maprs767215758
PheGenIrs767215758
hapmaprs767215758
1000 genomesrs767215758
hgdprs767215758
ensemblrs767215758
gopubmedrs767215758
geneviewrs767215758
scholarrs767215758
googlers767215758
pharmgkbrs767215758
gwascentralrs767215758
openSNPrs767215758
23andMers767215758
23andMe allrs767215758
SNP Nexus

SNPshotrs767215758
SNPdbers767215758
MSV3drs767215758
GWAS Ctlgrs767215758
Max Magnitude0
ClinVar
Risk rs767215758(A;A)
Alt rs767215758(A;A)
Reference rs767215758(G;G)
Significance Pathogenic
Disease Microcephaly not provided
Variation info
Gene NBN
CLNDBN Microcephaly, normal intelligence and immunodeficiency not provided
Reversed 0
HGVS NC_000008.10:g.90971047G>A
CLNSRC
CLNACC RCV000170446.1, RCV000170448.1, RCV000220210.1,