rs587782344

Orientation

minus

Stabilized

minus

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

Make rs587782344(-;A)

Make rs587782344(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

89953538

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs587782344
dbSNP (classic)	rs587782344
ClinGen	rs587782344
ebi	rs587782344
HLI	rs587782344
Exac	rs587782344
Gnomad	rs587782344
Varsome	rs587782344
LitVar	rs587782344
Map	rs587782344
PheGenI	rs587782344
Biobank	rs587782344
1000 genomes	rs587782344
hgdp	rs587782344
ensembl	rs587782344
geneview	rs587782344
scholar	rs587782344
google	rs587782344
pharmgkb	rs587782344
gwascentral	rs587782344
openSNP	rs587782344
23andMe	rs587782344
SNPshot	rs587782344
SNPdbe	rs587782344
MSV3d	rs587782344
GWAS Ctlg	rs587782344

Max Magnitude

0

ClinVar
Risk	rs587782344(A;A)
Alt	rs587782344(A;A)
Reference	Rs587782344(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	NBN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000008.10:g.90965767dupT
CLNSRC
CLNACC	RCV000131283.2,