rs587782130

Orientation

minus

Stabilized

minus

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

Make rs587782130(C;T)

Make rs587782130(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

89953615

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs587782130
dbSNP (classic)	rs587782130
ClinGen	rs587782130
ebi	rs587782130
HLI	rs587782130
Exac	rs587782130
Gnomad	rs587782130
Varsome	rs587782130
LitVar	rs587782130
Map	rs587782130
PheGenI	rs587782130
Biobank	rs587782130
1000 genomes	rs587782130
hgdp	rs587782130
ensembl	rs587782130
geneview	rs587782130
scholar	rs587782130
google	rs587782130
pharmgkb	rs587782130
gwascentral	rs587782130
openSNP	rs587782130
23andMe	rs587782130
SNPshot	rs587782130
SNPdbe	rs587782130
MSV3d	rs587782130
GWAS Ctlg	rs587782130

Max Magnitude

0

ClinVar
Risk	rs587782130(A;A) rs587782130(T;T)
Alt	rs587782130(A;A) rs587782130(T;T)
Reference	Rs587782130(C;C)
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.90965843G>A; NC_000008.10:g.90965843G>T
CLNSRC
CLNACC	RCV000130673.3, RCV000480769.1, RCV000213507.1,