rs775069541

Orientation

plus

Stabilized

plus

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

Make rs775069541(G;G)

Make rs775069541(G;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132618277

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs775069541
dbSNP (classic)	rs775069541
ClinGen	rs775069541
ebi	rs775069541
HLI	rs775069541
Exac	rs775069541
Gnomad	rs775069541
Varsome	rs775069541
LitVar	rs775069541
Map	rs775069541
PheGenI	rs775069541
Biobank	rs775069541
1000 genomes	rs775069541
hgdp	rs775069541
ensembl	rs775069541
geneview	rs775069541
scholar	rs775069541
google	rs775069541
pharmgkb	rs775069541
gwascentral	rs775069541
openSNP	rs775069541
23andMe	rs775069541
SNPshot	rs775069541
SNPdbe	rs775069541
MSV3d	rs775069541
GWAS Ctlg	rs775069541

Max Magnitude

0

ClinVar
Risk	rs775069541(A;A) rs775069541(G;G)
Alt	rs775069541(A;A) rs775069541(G;G)
Reference	Rs775069541(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131953969T>A
CLNSRC
CLNACC	RCV000218193.1,