rs876661189

Orientation

minus

Stabilized

minus

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

Make rs876661189(-;TT)

Make rs876661189(TT;TT)

Reference

GRCh38.p2 38.2/147

Chromosome

8

Position

89943327

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs876661189
dbSNP (classic)	rs876661189
ClinGen	rs876661189
ebi	rs876661189
HLI	rs876661189
Exac	rs876661189
Gnomad	rs876661189
Varsome	rs876661189
LitVar	rs876661189
Map	rs876661189
PheGenI	rs876661189
Biobank	rs876661189
1000 genomes	rs876661189
hgdp	rs876661189
ensembl	rs876661189
geneview	rs876661189
scholar	rs876661189
google	rs876661189
pharmgkb	rs876661189
gwascentral	rs876661189
openSNP	rs876661189
23andMe	rs876661189
SNPshot	rs876661189
SNPdbe	rs876661189
MSV3d	rs876661189
GWAS Ctlg	rs876661189

Max Magnitude

0

ClinVar
Risk	rs876661189(TT;TT)
Alt	rs876661189(TT;TT)
Reference	Rs876661189(-;-)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NBN
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.90955556_90955557dupAA
CLNSRC
CLNACC	RCV000220883.1,