rs587781327

Orientation

plus

Stabilized

plus

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

Make rs587781327(-;-)

Make rs587781327(-;CT)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

132589653

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs587781327
dbSNP (classic)	rs587781327
ClinGen	rs587781327
ebi	rs587781327
HLI	rs587781327
Exac	rs587781327
Gnomad	rs587781327
Varsome	rs587781327
LitVar	rs587781327
Map	rs587781327
PheGenI	rs587781327
Biobank	rs587781327
1000 genomes	rs587781327
hgdp	rs587781327
ensembl	rs587781327
geneview	rs587781327
scholar	rs587781327
google	rs587781327
pharmgkb	rs587781327
gwascentral	rs587781327
openSNP	rs587781327
23andMe	rs587781327
SNPshot	rs587781327
SNPdbe	rs587781327
MSV3d	rs587781327
GWAS Ctlg	rs587781327

Merged from

Rs786203738

Max Magnitude

0

ClinVar
Risk	rs587781327(-;-)
Alt	rs587781327(-;-)
Reference	Rs587781327(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,