rs397507177

Orientation

plus

Stabilized

plus

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

Make rs397507177(C;T)

Make rs397507177(T;T)

Reference

GRCh38 38.1/141

Chromosome

5

Position

132608717

Gene

RAD50

is a	snp
is	mentioned by
dbSNP	rs397507177
dbSNP (classic)	rs397507177
ClinGen	rs397507177
ebi	rs397507177
HLI	rs397507177
Exac	rs397507177
Gnomad	rs397507177
Varsome	rs397507177
LitVar	rs397507177
Map	rs397507177
PheGenI	rs397507177
Biobank	rs397507177
1000 genomes	rs397507177
hgdp	rs397507177
ensembl	rs397507177
geneview	rs397507177
scholar	rs397507177
google	rs397507177
pharmgkb	rs397507177
gwascentral	rs397507177
openSNP	rs397507177
23andMe	rs397507177
SNPshot	rs397507177
SNPdbe	rs397507177
MSV3d	rs397507177
GWAS Ctlg	rs397507177

Max Magnitude

0

ClinVar
Risk	rs397507177(T;T)
Alt	rs397507177(T;T)
Reference	Rs397507177(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.131944409C>T
CLNSRC	Ambry Genetics ClinVar
CLNACC	RCV000030957.4,