rs876660039

Orientation

plus

Stabilized

plus

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

Make rs876660039(-;-)

Make rs876660039(-;C)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132588809

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs876660039
dbSNP (classic)	rs876660039
ClinGen	rs876660039
ebi	rs876660039
HLI	rs876660039
Exac	rs876660039
Gnomad	rs876660039
Varsome	rs876660039
LitVar	rs876660039
Map	rs876660039
PheGenI	rs876660039
Biobank	rs876660039
1000 genomes	rs876660039
hgdp	rs876660039
ensembl	rs876660039
geneview	rs876660039
scholar	rs876660039
google	rs876660039
pharmgkb	rs876660039
gwascentral	rs876660039
openSNP	rs876660039
23andMe	rs876660039
SNPshot	rs876660039
SNPdbe	rs876660039
MSV3d	rs876660039
GWAS Ctlg	rs876660039

Max Magnitude

0

ClinVar
Risk	rs876660039(-;-)
Alt	rs876660039(-;-)
Reference	Rs876660039(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131924501delC
CLNSRC
CLNACC	RCV000214856.1,