rs786201789

Orientation

plus

Stabilized

plus

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

Make rs786201789(-;-)

Make rs786201789(-;C)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

132595805

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs786201789
dbSNP (classic)	rs786201789
ClinGen	rs786201789
ebi	rs786201789
HLI	rs786201789
Exac	rs786201789
Gnomad	rs786201789
Varsome	rs786201789
LitVar	rs786201789
Map	rs786201789
PheGenI	rs786201789
Biobank	rs786201789
1000 genomes	rs786201789
hgdp	rs786201789
ensembl	rs786201789
geneview	rs786201789
scholar	rs786201789
google	rs786201789
pharmgkb	rs786201789
gwascentral	rs786201789
openSNP	rs786201789
23andMe	rs786201789
SNPshot	rs786201789
SNPdbe	rs786201789
MSV3d	rs786201789
GWAS Ctlg	rs786201789

Max Magnitude

0

ClinVar
Risk	rs786201789(-;-)
Alt	rs786201789(-;-)
Reference	Rs786201789(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.131931497delC
CLNSRC
CLNACC	RCV000164257.4,