rs745797941

Orientation

plus

Stabilized

plus

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

Make rs745797941(C;T)

Make rs745797941(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132637179

Gene	RAD50, TH2LCRR

is a	snp
is	mentioned by
dbSNP	rs745797941
dbSNP (classic)	rs745797941
ClinGen	rs745797941
ebi	rs745797941
HLI	rs745797941
Exac	rs745797941
Gnomad	rs745797941
Varsome	rs745797941
LitVar	rs745797941
Map	rs745797941
PheGenI	rs745797941
Biobank	rs745797941
1000 genomes	rs745797941
hgdp	rs745797941
ensembl	rs745797941
geneview	rs745797941
scholar	rs745797941
google	rs745797941
pharmgkb	rs745797941
gwascentral	rs745797941
openSNP	rs745797941
23andMe	rs745797941
SNPshot	rs745797941
SNPdbe	rs745797941
MSV3d	rs745797941
GWAS Ctlg	rs745797941

Max Magnitude

0

ClinVar
Risk	rs745797941(T;T)
Alt	rs745797941(T;T)
Reference	Rs745797941(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	TH2LCRR RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131972871C>T
CLNSRC
CLNACC	RCV000222027.1,