rs587782286

Orientation

plus

Stabilized

plus

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

Make rs587782286(-;-)

Make rs587782286(-;AG)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58703275

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587782286
dbSNP (classic)	rs587782286
ClinGen	rs587782286
ebi	rs587782286
HLI	rs587782286
Exac	rs587782286
Gnomad	rs587782286
Varsome	rs587782286
LitVar	rs587782286
Map	rs587782286
PheGenI	rs587782286
Biobank	rs587782286
1000 genomes	rs587782286
hgdp	rs587782286
ensembl	rs587782286
geneview	rs587782286
scholar	rs587782286
google	rs587782286
pharmgkb	rs587782286
gwascentral	rs587782286
openSNP	rs587782286
23andMe	rs587782286
SNPshot	rs587782286
SNPdbe	rs587782286
MSV3d	rs587782286
GWAS Ctlg	rs587782286

Merged from

Rs786203081

Max Magnitude

0

ClinVar
Risk	rs587782286(-;-)
Alt	rs587782286(-;-)
Reference	Rs587782286(AG;AG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56780638_56780639delAG
CLNSRC
CLNACC	RCV000166223.2,