rs587781305

Orientation

minus

Stabilized

minus

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

Make rs587781305(-;-)

Make rs587781305(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

89981389

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs587781305
dbSNP (classic)	rs587781305
ClinGen	rs587781305
ebi	rs587781305
HLI	rs587781305
Exac	rs587781305
Gnomad	rs587781305
Varsome	rs587781305
LitVar	rs587781305
Map	rs587781305
PheGenI	rs587781305
Biobank	rs587781305
1000 genomes	rs587781305
hgdp	rs587781305
ensembl	rs587781305
geneview	rs587781305
scholar	rs587781305
google	rs587781305
pharmgkb	rs587781305
gwascentral	rs587781305
openSNP	rs587781305
23andMe	rs587781305
SNPshot	rs587781305
SNPdbe	rs587781305
MSV3d	rs587781305
GWAS Ctlg	rs587781305

Max Magnitude

0

ClinVar
Risk	rs587781305(-;-)
Alt	rs587781305(-;-)
Reference	Rs587781305(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	NBN
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000008.10:g.90993617delA
CLNSRC
CLNACC	RCV000129019.2, RCV000478932.1,