rs368980595

Orientation

plus

Stabilized

plus

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

Make rs368980595(C;T)

Make rs368980595(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

5

Position

132618134

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs368980595
dbSNP (classic)	rs368980595
ClinGen	rs368980595
ebi	rs368980595
HLI	rs368980595
Exac	rs368980595
Gnomad	rs368980595
Varsome	rs368980595
LitVar	rs368980595
Map	rs368980595
PheGenI	rs368980595
Biobank	rs368980595
1000 genomes	rs368980595
hgdp	rs368980595
ensembl	rs368980595
geneview	rs368980595
scholar	rs368980595
google	rs368980595
pharmgkb	rs368980595
gwascentral	rs368980595
openSNP	rs368980595
23andMe	rs368980595
SNPshot	rs368980595
SNPdbe	rs368980595
MSV3d	rs368980595
GWAS Ctlg	rs368980595

Max Magnitude

0

ClinVar
Risk	rs368980595(A;A) rs368980595(T;T)
Alt	rs368980595(A;A) rs368980595(T;T)
Reference	Rs368980595(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD50
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000005.9:g.131953826C>A; NC_000005.9:g.131953826C>T
CLNSRC
CLNACC	RCV000219691.1, RCV000217668.1,