rs730881840

Orientation

minus

Stabilized

minus

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

Make rs730881840(-;-)

Make rs730881840(-;TGAAAATGATCAGTCGATCAGCCGAAATCAT)

Reference

GRCh38.p2 38.2/144

Chromosome

8

Position

89982758

Gene

NBN

is a	snp
is	mentioned by
dbSNP	rs730881840
dbSNP (classic)	rs730881840
ClinGen	rs730881840
ebi	rs730881840
HLI	rs730881840
Exac	rs730881840
Gnomad	rs730881840
Varsome	rs730881840
LitVar	rs730881840
Map	rs730881840
PheGenI	rs730881840
Biobank	rs730881840
1000 genomes	rs730881840
hgdp	rs730881840
ensembl	rs730881840
geneview	rs730881840
scholar	rs730881840
google	rs730881840
pharmgkb	rs730881840
gwascentral	rs730881840
openSNP	rs730881840
23andMe	rs730881840
SNPshot	rs730881840
SNPdbe	rs730881840
MSV3d	rs730881840
GWAS Ctlg	rs730881840

Max Magnitude

0

ClinVar
Risk	rs730881840(-;-)
Alt	rs730881840(-;-)
Reference	Rs730881840(TGAAAATGATCAGTCGATCAGCCGAAATCAT;TGAAAATGATCAGTCGATCAGCCGAAATCAT)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	NBN
CLNDBN	not provided
Reversed	1
HGVS	NC_000008.10:g.90994986_90995016del31
CLNSRC
CLNACC	RCV000160767.2,