rs587781742

Orientation

plus

Stabilized

plus

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

Make rs587781742(G;T)

Make rs587781742(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

132594868

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs587781742
dbSNP (classic)	rs587781742
ClinGen	rs587781742
ebi	rs587781742
HLI	rs587781742
Exac	rs587781742
Gnomad	rs587781742
Varsome	rs587781742
LitVar	rs587781742
Map	rs587781742
PheGenI	rs587781742
Biobank	rs587781742
1000 genomes	rs587781742
hgdp	rs587781742
ensembl	rs587781742
geneview	rs587781742
scholar	rs587781742
google	rs587781742
pharmgkb	rs587781742
gwascentral	rs587781742
openSNP	rs587781742
23andMe	rs587781742
SNPshot	rs587781742
SNPdbe	rs587781742
MSV3d	rs587781742
GWAS Ctlg	rs587781742

Max Magnitude

0

ClinVar
Risk	rs587781742(A;A) rs587781742(T;T)
Alt	rs587781742(A;A) rs587781742(T;T)
Reference	Rs587781742(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131930560G>T
CLNSRC
CLNACC	RCV000129946.3,