rs587781576

Orientation

plus

Stabilized

plus

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

Make rs587781576(C;T)

Make rs587781576(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

132579953

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs587781576
dbSNP (classic)	rs587781576
ClinGen	rs587781576
ebi	rs587781576
HLI	rs587781576
Exac	rs587781576
Gnomad	rs587781576
Varsome	rs587781576
LitVar	rs587781576
Map	rs587781576
PheGenI	rs587781576
Biobank	rs587781576
1000 genomes	rs587781576
hgdp	rs587781576
ensembl	rs587781576
geneview	rs587781576
scholar	rs587781576
google	rs587781576
pharmgkb	rs587781576
gwascentral	rs587781576
openSNP	rs587781576
23andMe	rs587781576
SNPshot	rs587781576
SNPdbe	rs587781576
MSV3d	rs587781576
GWAS Ctlg	rs587781576

Max Magnitude

0

ClinVar
Risk	rs587781576(T;T)
Alt	rs587781576(T;T)
Reference	Rs587781576(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.131915645C>T
CLNSRC
CLNACC	RCV000129612.2,