rs786203738

Merged into

rs587781327

Orientation

plus

Stabilized

plus

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

Make rs786203738(-;-)

Make rs786203738(-;CT)

Reference

GRCh38.p2 38.2/146

Chromosome

5

Position

132589655

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs786203738
dbSNP (classic)	rs786203738
ClinGen	rs786203738
ebi	rs786203738
HLI	rs786203738
Exac	rs786203738
Gnomad	rs786203738
Varsome	rs786203738
LitVar	rs786203738
Map	rs786203738
PheGenI	rs786203738
Biobank	rs786203738
1000 genomes	rs786203738
hgdp	rs786203738
ensembl	rs786203738
geneview	rs786203738
scholar	rs786203738
google	rs786203738
pharmgkb	rs786203738
gwascentral	rs786203738
openSNP	rs786203738
23andMe	rs786203738
SNPshot	rs786203738
SNPdbe	rs786203738
MSV3d	rs786203738
GWAS Ctlg	rs786203738

Status

Merged into rs587781327

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs786203738(CT;CT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131925347_131925348delCT
CLNSRC
CLNACC	RCV000167173.4,