rs1057516332

Orientation

minus

Stabilized

minus

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

Make rs1057516332(-;A)

Make rs1057516332(A;A)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

89953501

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs1057516332
dbSNP (classic)	rs1057516332
ClinGen	rs1057516332
ebi	rs1057516332
HLI	rs1057516332
Exac	rs1057516332
Gnomad	rs1057516332
Varsome	rs1057516332
LitVar	rs1057516332
Map	rs1057516332
PheGenI	rs1057516332
Biobank	rs1057516332
1000 genomes	rs1057516332
hgdp	rs1057516332
ensembl	rs1057516332
geneview	rs1057516332
scholar	rs1057516332
google	rs1057516332
pharmgkb	rs1057516332
gwascentral	rs1057516332
openSNP	rs1057516332
23andMe	rs1057516332
SNPshot	rs1057516332
SNPdbe	rs1057516332
MSV3d	rs1057516332
GWAS Ctlg	rs1057516332

Max Magnitude

0

ClinVar
Risk	rs1057516332(A;A)
Alt	rs1057516332(A;A)
Reference	Rs1057516332(-;-)
Significance	Probable-Pathogenic
Disease	Microcephaly
Variation	info
Gene	NBN
CLNDBN	Microcephaly, normal intelligence and immunodeficiency
Reversed	1
HGVS	NC_000008.10:g.90965730dupT
CLNSRC
CLNACC	RCV000410169.1,