rs786203920

Orientation

minus

Stabilized

minus

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

Make rs786203920(A;T)

Make rs786203920(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

89946154

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs786203920
dbSNP (classic)	rs786203920
ClinGen	rs786203920
ebi	rs786203920
HLI	rs786203920
Exac	rs786203920
Gnomad	rs786203920
Varsome	rs786203920
LitVar	rs786203920
Map	rs786203920
PheGenI	rs786203920
Biobank	rs786203920
1000 genomes	rs786203920
hgdp	rs786203920
ensembl	rs786203920
geneview	rs786203920
scholar	rs786203920
google	rs786203920
pharmgkb	rs786203920
gwascentral	rs786203920
openSNP	rs786203920
23andMe	rs786203920
SNPshot	rs786203920
SNPdbe	rs786203920
MSV3d	rs786203920
GWAS Ctlg	rs786203920

Max Magnitude

0

ClinVar
Risk	rs786203920(T;T)
Alt	rs786203920(T;T)
Reference	Rs786203920(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	NBN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000008.10:g.90958382T>A
CLNSRC
CLNACC	RCV000167435.1,