rs786203180

Orientation

minus

Stabilized

minus

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

Make rs786203180(A;A)

Make rs786203180(A;CC)

Reference

GRCh38.p2 38.2/146

Chromosome

8

Position

89953605

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs786203180
dbSNP (classic)	rs786203180
ClinGen	rs786203180
ebi	rs786203180
HLI	rs786203180
Exac	rs786203180
Gnomad	rs786203180
Varsome	rs786203180
LitVar	rs786203180
Map	rs786203180
PheGenI	rs786203180
Biobank	rs786203180
1000 genomes	rs786203180
hgdp	rs786203180
ensembl	rs786203180
geneview	rs786203180
scholar	rs786203180
google	rs786203180
pharmgkb	rs786203180
gwascentral	rs786203180
openSNP	rs786203180
23andMe	rs786203180
SNPshot	rs786203180
SNPdbe	rs786203180
MSV3d	rs786203180
GWAS Ctlg	rs786203180

Max Magnitude

0

ClinVar
Risk	rs786203180(A;A)
Alt	rs786203180(A;A)
Reference	Rs786203180(CC;CC)
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.90965833_90965834delGGinsT
CLNSRC
CLNACC	RCV000166379.2, RCV000482780.1,