rs587781925

Orientation

plus

Stabilized

plus

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

Make rs587781925(A;A)

Make rs587781925(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

5

Position

132638224

Gene	RAD50, TH2LCRR

is a	snp
is	mentioned by
dbSNP	rs587781925
dbSNP (classic)	rs587781925
ClinGen	rs587781925
ebi	rs587781925
HLI	rs587781925
Exac	rs587781925
Gnomad	rs587781925
Varsome	rs587781925
LitVar	rs587781925
Map	rs587781925
PheGenI	rs587781925
Biobank	rs587781925
1000 genomes	rs587781925
hgdp	rs587781925
ensembl	rs587781925
geneview	rs587781925
scholar	rs587781925
google	rs587781925
pharmgkb	rs587781925
gwascentral	rs587781925
openSNP	rs587781925
23andMe	rs587781925
SNPshot	rs587781925
SNPdbe	rs587781925
MSV3d	rs587781925
GWAS Ctlg	rs587781925

Max Magnitude

0

ClinVar
Risk	rs587781925(A;A)
Alt	rs587781925(A;A)
Reference	Rs587781925(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	LOC101927761 TH2LCRR RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131973916G>A
CLNSRC
CLNACC	RCV000130277.3,