rs786203223

Orientation

minus

Stabilized

minus

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

Make rs786203223(G;G)

Make rs786203223(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

89946138

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs786203223
dbSNP (classic)	rs786203223
ClinGen	rs786203223
ebi	rs786203223
HLI	rs786203223
Exac	rs786203223
Gnomad	rs786203223
Varsome	rs786203223
LitVar	rs786203223
Map	rs786203223
PheGenI	rs786203223
Biobank	rs786203223
1000 genomes	rs786203223
hgdp	rs786203223
ensembl	rs786203223
geneview	rs786203223
scholar	rs786203223
google	rs786203223
pharmgkb	rs786203223
gwascentral	rs786203223
openSNP	rs786203223
23andMe	rs786203223
SNPshot	rs786203223
SNPdbe	rs786203223
MSV3d	rs786203223
GWAS Ctlg	rs786203223

Max Magnitude

0

ClinVar
Risk	rs786203223(G;G)
Alt	rs786203223(G;G)
Reference	Rs786203223(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	NBN
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000008.10:g.90958366A>C
CLNSRC
CLNACC	RCV000166440.2,