rs876658976

Orientation

plus

Stabilized

plus

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

Make rs876658976(-;T)

Make rs876658976(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132608640

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs876658976
dbSNP (classic)	rs876658976
ClinGen	rs876658976
ebi	rs876658976
HLI	rs876658976
Exac	rs876658976
Gnomad	rs876658976
Varsome	rs876658976
LitVar	rs876658976
Map	rs876658976
PheGenI	rs876658976
Biobank	rs876658976
1000 genomes	rs876658976
hgdp	rs876658976
ensembl	rs876658976
geneview	rs876658976
scholar	rs876658976
google	rs876658976
pharmgkb	rs876658976
gwascentral	rs876658976
openSNP	rs876658976
23andMe	rs876658976
SNPshot	rs876658976
SNPdbe	rs876658976
MSV3d	rs876658976
GWAS Ctlg	rs876658976

Max Magnitude

0

ClinVar
Risk	rs876658976(T;T)
Alt	rs876658976(T;T)
Reference	Rs876658976(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131944332dupT
CLNSRC
CLNACC	RCV000217594.1,