rs730881839

Orientation

minus

Stabilized

minus

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

Make rs730881839(-;A)

Make rs730881839(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

89970442

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs730881839
dbSNP (classic)	rs730881839
ClinGen	rs730881839
ebi	rs730881839
HLI	rs730881839
Exac	rs730881839
Gnomad	rs730881839
Varsome	rs730881839
LitVar	rs730881839
Map	rs730881839
PheGenI	rs730881839
Biobank	rs730881839
1000 genomes	rs730881839
hgdp	rs730881839
ensembl	rs730881839
geneview	rs730881839
scholar	rs730881839
google	rs730881839
pharmgkb	rs730881839
gwascentral	rs730881839
openSNP	rs730881839
23andMe	rs730881839
SNPshot	rs730881839
SNPdbe	rs730881839
MSV3d	rs730881839
GWAS Ctlg	rs730881839

Max Magnitude

0

ClinVar
Risk	rs730881839(A;A)
Alt	rs730881839(A;A)
Reference	Rs730881839(-;-)
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.90982671dupT
CLNSRC
CLNACC	RCV000160766.2, RCV000258971.2,