rs761168506

Orientation

plus

Stabilized

plus

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

Make rs761168506(C;C)

Make rs761168506(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132637202

Gene	RAD50, TH2LCRR

is a	snp
is	mentioned by
dbSNP	rs761168506
dbSNP (classic)	rs761168506
ClinGen	rs761168506
ebi	rs761168506
HLI	rs761168506
Exac	rs761168506
Gnomad	rs761168506
Varsome	rs761168506
LitVar	rs761168506
Map	rs761168506
PheGenI	rs761168506
Biobank	rs761168506
1000 genomes	rs761168506
hgdp	rs761168506
ensembl	rs761168506
geneview	rs761168506
scholar	rs761168506
google	rs761168506
pharmgkb	rs761168506
gwascentral	rs761168506
openSNP	rs761168506
23andMe	rs761168506
SNPshot	rs761168506
SNPdbe	rs761168506
MSV3d	rs761168506
GWAS Ctlg	rs761168506

Max Magnitude

0

ClinVar
Risk	rs761168506(C;C)
Alt	rs761168506(C;C)
Reference	Rs761168506(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TH2LCRR RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131972894T>C
CLNSRC
CLNACC	RCV000223053.1,