rs876659837

Orientation

plus

Stabilized

plus

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

Make rs876659837(-;-)

Make rs876659837(-;A)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132559308

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs876659837
dbSNP (classic)	rs876659837
ClinGen	rs876659837
ebi	rs876659837
HLI	rs876659837
Exac	rs876659837
Gnomad	rs876659837
Varsome	rs876659837
LitVar	rs876659837
Map	rs876659837
PheGenI	rs876659837
Biobank	rs876659837
1000 genomes	rs876659837
hgdp	rs876659837
ensembl	rs876659837
geneview	rs876659837
scholar	rs876659837
google	rs876659837
pharmgkb	rs876659837
gwascentral	rs876659837
openSNP	rs876659837
23andMe	rs876659837
SNPshot	rs876659837
SNPdbe	rs876659837
MSV3d	rs876659837
GWAS Ctlg	rs876659837

Max Magnitude

0

ClinVar
Risk	rs876659837(-;-)
Alt	rs876659837(-;-)
Reference	Rs876659837(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131895000delA
CLNSRC
CLNACC	RCV000220905.1,