rs786203081

Merged into

rs587782286

Orientation

plus

Stabilized

plus

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

Make rs786203081(-;-)

Make rs786203081(-;AG)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

58703277

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs786203081
dbSNP (classic)	rs786203081
ClinGen	rs786203081
ebi	rs786203081
HLI	rs786203081
Exac	rs786203081
Gnomad	rs786203081
Varsome	rs786203081
LitVar	rs786203081
Map	rs786203081
PheGenI	rs786203081
Biobank	rs786203081
1000 genomes	rs786203081
hgdp	rs786203081
ensembl	rs786203081
geneview	rs786203081
scholar	rs786203081
google	rs786203081
pharmgkb	rs786203081
gwascentral	rs786203081
openSNP	rs786203081
23andMe	rs786203081
SNPshot	rs786203081
SNPdbe	rs786203081
MSV3d	rs786203081
GWAS Ctlg	rs786203081

Status

Merged into rs587782286

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs786203081(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,