rs587780096

Orientation

minus

Stabilized

minus

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

Make rs587780096(C;C)

Make rs587780096(C;G)

Reference

GRCh38.p7 38.3/150

Chromosome

8

Position

89980889

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs587780096
dbSNP (classic)	rs587780096
ClinGen	rs587780096
ebi	rs587780096
HLI	rs587780096
Exac	rs587780096
Gnomad	rs587780096
Varsome	rs587780096
LitVar	rs587780096
Map	rs587780096
PheGenI	rs587780096
Biobank	rs587780096
1000 genomes	rs587780096
hgdp	rs587780096
ensembl	rs587780096
geneview	rs587780096
scholar	rs587780096
google	rs587780096
pharmgkb	rs587780096
gwascentral	rs587780096
openSNP	rs587780096
23andMe	rs587780096
SNPshot	rs587780096
SNPdbe	rs587780096
MSV3d	rs587780096
GWAS Ctlg	rs587780096

Max Magnitude

0

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,