rs1064795634

Orientation

minus

Stabilized

minus

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

Chromosome

8

Position

89981480

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs1064795634
dbSNP (classic)	rs1064795634
ClinGen	rs1064795634
ebi	rs1064795634
HLI	rs1064795634
Exac	rs1064795634
Gnomad	rs1064795634
Varsome	rs1064795634
LitVar	rs1064795634
Map	rs1064795634
PheGenI	rs1064795634
Biobank	rs1064795634
1000 genomes	rs1064795634
hgdp	rs1064795634
ensembl	rs1064795634
geneview	rs1064795634
scholar	rs1064795634
google	rs1064795634
pharmgkb	rs1064795634
gwascentral	rs1064795634
openSNP	rs1064795634
23andMe	rs1064795634
SNPshot	rs1064795634
SNPdbe	rs1064795634
MSV3d	rs1064795634
GWAS Ctlg	rs1064795634

Max Magnitude

0

ClinVar
Risk	rs1064795634(-;-)
Alt	rs1064795634(-;-)
Reference	Rs1064795634(ATTC;ATTC)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	NBN
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.90993708_90993711delGAAT
CLNSRC
CLNACC	RCV000478442.1,