rs767215758

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(G;G)	0	common in clinvar

Make rs767215758(A;A)

Make rs767215758(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

89958819

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs767215758
dbSNP (classic)	rs767215758
ClinGen	rs767215758
ebi	rs767215758
HLI	rs767215758
Exac	rs767215758
Gnomad	rs767215758
Varsome	rs767215758
LitVar	rs767215758
Map	rs767215758
PheGenI	rs767215758
Biobank	rs767215758
1000 genomes	rs767215758
hgdp	rs767215758
ensembl	rs767215758
geneview	rs767215758
scholar	rs767215758
google	rs767215758
pharmgkb	rs767215758
gwascentral	rs767215758
openSNP	rs767215758
23andMe	rs767215758
SNPshot	rs767215758
SNPdbe	rs767215758
MSV3d	rs767215758
GWAS Ctlg	rs767215758

Max Magnitude

0

ClinVar
Risk	rs767215758(A;A)
Alt	rs767215758(A;A)
Reference	Rs767215758(G;G)
Significance	Other
Disease	Microcephaly not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	NBN
CLNDBN	Microcephaly, normal intelligence and immunodeficiency not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000008.10:g.90971047G>A
CLNSRC
CLNACC	RCV000170446.1, RCV000170448.1, RCV000220210.1, RCV000446931.1,