rs730881939

Orientation

plus

Stabilized

plus

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

Make rs730881939(-;A)

Make rs730881939(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58695009

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs730881939
dbSNP (classic)	rs730881939
ClinGen	rs730881939
ebi	rs730881939
HLI	rs730881939
Exac	rs730881939
Gnomad	rs730881939
Varsome	rs730881939
LitVar	rs730881939
Map	rs730881939
PheGenI	rs730881939
Biobank	rs730881939
1000 genomes	rs730881939
hgdp	rs730881939
ensembl	rs730881939
geneview	rs730881939
scholar	rs730881939
google	rs730881939
pharmgkb	rs730881939
gwascentral	rs730881939
openSNP	rs730881939
23andMe	rs730881939
SNPshot	rs730881939
SNPdbe	rs730881939
MSV3d	rs730881939
GWAS Ctlg	rs730881939

Max Magnitude

0

ClinVar
Risk	rs730881939(A;A)
Alt	rs730881939(A;A)
Reference	Rs730881939(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not provided Breast-ovarian cancer
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided Breast-ovarian cancer, familial 3
Reversed	0
HGVS	NC_000017.10:g.56772370dupA
CLNSRC
CLNACC	RCV000160933.4, RCV000206050.2, RCV000258982.2, RCV000409268.1,