rs587782170

Orientation

plus

Stabilized

plus

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

Make rs587782170(-;-)

Make rs587782170(-;AA)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58694971

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587782170
dbSNP (classic)	rs587782170
ClinGen	rs587782170
ebi	rs587782170
HLI	rs587782170
Exac	rs587782170
Gnomad	rs587782170
Varsome	rs587782170
LitVar	rs587782170
Map	rs587782170
PheGenI	rs587782170
Biobank	rs587782170
1000 genomes	rs587782170
hgdp	rs587782170
ensembl	rs587782170
geneview	rs587782170
scholar	rs587782170
google	rs587782170
pharmgkb	rs587782170
gwascentral	rs587782170
openSNP	rs587782170
23andMe	rs587782170
SNPshot	rs587782170
SNPdbe	rs587782170
MSV3d	rs587782170
GWAS Ctlg	rs587782170

Max Magnitude

0

ClinVar
Risk	rs587782170(-;-)
Alt	rs587782170(-;-)
Reference	Rs587782170(AA;AA)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O
Reversed	0
HGVS	NC_000017.10:g.56772332_56772333delAA
CLNSRC
CLNACC	RCV000130769.2, RCV000459126.1,