rs876659654

Orientation

plus

Stabilized

plus

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

Make rs876659654(C;T)

Make rs876659654(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132642212

Gene	RAD50, TH2LCRR

is a	snp
is	mentioned by
dbSNP	rs876659654
dbSNP (classic)	rs876659654
ClinGen	rs876659654
ebi	rs876659654
HLI	rs876659654
Exac	rs876659654
Gnomad	rs876659654
Varsome	rs876659654
LitVar	rs876659654
Map	rs876659654
PheGenI	rs876659654
Biobank	rs876659654
1000 genomes	rs876659654
hgdp	rs876659654
ensembl	rs876659654
geneview	rs876659654
scholar	rs876659654
google	rs876659654
pharmgkb	rs876659654
gwascentral	rs876659654
openSNP	rs876659654
23andMe	rs876659654
SNPshot	rs876659654
SNPdbe	rs876659654
MSV3d	rs876659654
GWAS Ctlg	rs876659654

Max Magnitude

0

ClinVar
Risk	rs876659654(T;T)
Alt	rs876659654(T;T)
Reference	Rs876659654(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	LOC101927761 TH2LCRR RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131977904C>T
CLNSRC
CLNACC	RCV000222239.1,