rs587781355

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(GT;GT)	0	common in clinvar
(I;I)	0	common genotype
(TG;TG)	0	common in clinvar

Make rs587781355(-;-)

Make rs587781355(-;TG)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

132579350

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs587781355
dbSNP (classic)	rs587781355
ClinGen	rs587781355
ebi	rs587781355
HLI	rs587781355
Exac	rs587781355
Gnomad	rs587781355
Varsome	rs587781355
LitVar	rs587781355
Map	rs587781355
PheGenI	rs587781355
Biobank	rs587781355
1000 genomes	rs587781355
hgdp	rs587781355
ensembl	rs587781355
geneview	rs587781355
scholar	rs587781355
google	rs587781355
pharmgkb	rs587781355
gwascentral	rs587781355
openSNP	rs587781355
23andMe	rs587781355
SNPshot	rs587781355
SNPdbe	rs587781355
MSV3d	rs587781355
GWAS Ctlg	rs587781355

Max Magnitude

0

ClinVar
Risk	rs587781355(-;-) Rs587781355(GT;GT)
Alt	rs587781355(-;-) Rs587781355(GT;GT)
Reference	Rs587781355(TG;TG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131915042_131915043delTG
CLNSRC
CLNACC	RCV000129139.4,