rs587781454

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(A;A)	0	common in clinvar

Make rs587781454(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

132595768

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs587781454
dbSNP (classic)	rs587781454
ClinGen	rs587781454
ebi	rs587781454
HLI	rs587781454
Exac	rs587781454
Gnomad	rs587781454
Varsome	rs587781454
LitVar	rs587781454
Map	rs587781454
PheGenI	rs587781454
Biobank	rs587781454
1000 genomes	rs587781454
hgdp	rs587781454
ensembl	rs587781454
geneview	rs587781454
scholar	rs587781454
google	rs587781454
pharmgkb	rs587781454
gwascentral	rs587781454
openSNP	rs587781454
23andMe	rs587781454
SNPshot	rs587781454
SNPdbe	rs587781454
MSV3d	rs587781454
GWAS Ctlg	rs587781454

Max Magnitude

0

ClinVar
Risk	Rs587781454(A;A) rs587781454(T;T)
Alt	Rs587781454(A;A) rs587781454(T;T)
Reference	Rs587781454(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131931460_131931461insT; NC_000005.9:g.131931460dupA
CLNSRC
CLNACC	RCV000469803.1, RCV000129381.7,