rs776276760

Orientation

plus

Stabilized

plus

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

Make rs776276760(C;G)

Make rs776276760(G;G)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132588882

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs776276760
dbSNP (classic)	rs776276760
ClinGen	rs776276760
ebi	rs776276760
HLI	rs776276760
Exac	rs776276760
Gnomad	rs776276760
Varsome	rs776276760
LitVar	rs776276760
Map	rs776276760
PheGenI	rs776276760
Biobank	rs776276760
1000 genomes	rs776276760
hgdp	rs776276760
ensembl	rs776276760
geneview	rs776276760
scholar	rs776276760
google	rs776276760
pharmgkb	rs776276760
gwascentral	rs776276760
openSNP	rs776276760
23andMe	rs776276760
SNPshot	rs776276760
SNPdbe	rs776276760
MSV3d	rs776276760
GWAS Ctlg	rs776276760

Max Magnitude

0

ClinVar
Risk	rs776276760(G;G)
Alt	rs776276760(G;G)
Reference	Rs776276760(C;C)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131924574C>G
CLNSRC
CLNACC	RCV000234702.1,