rs760146707

Orientation

plus

Stabilized

plus

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

Make rs760146707(-;-)

Make rs760146707(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

132579997

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs760146707
dbSNP (classic)	rs760146707
ClinGen	rs760146707
ebi	rs760146707
HLI	rs760146707
Exac	rs760146707
Gnomad	rs760146707
Varsome	rs760146707
LitVar	rs760146707
Map	rs760146707
PheGenI	rs760146707
Biobank	rs760146707
1000 genomes	rs760146707
hgdp	rs760146707
ensembl	rs760146707
geneview	rs760146707
scholar	rs760146707
google	rs760146707
pharmgkb	rs760146707
gwascentral	rs760146707
openSNP	rs760146707
23andMe	rs760146707
SNPshot	rs760146707
SNPdbe	rs760146707
MSV3d	rs760146707
GWAS Ctlg	rs760146707

Max Magnitude

0

ClinVar
Risk	rs760146707(-;-)
Alt	rs760146707(-;-)
Reference	Rs760146707(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Nijmegen breakage syndrome-like disorder
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome Nijmegen breakage syndrome-like disorder
Reversed	0
HGVS	NC_000005.9:g.131915689delT
CLNSRC
CLNACC	RCV000164362.1, RCV000409900.1,