rs760235677

Orientation

plus

Stabilized

plus

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

Make rs760235677(A;A)

Make rs760235677(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

58709991

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs760235677
dbSNP (classic)	rs760235677
ClinGen	rs760235677
ebi	rs760235677
HLI	rs760235677
Exac	rs760235677
Gnomad	rs760235677
Varsome	rs760235677
LitVar	rs760235677
Map	rs760235677
PheGenI	rs760235677
Biobank	rs760235677
1000 genomes	rs760235677
hgdp	rs760235677
ensembl	rs760235677
geneview	rs760235677
scholar	rs760235677
google	rs760235677
pharmgkb	rs760235677
gwascentral	rs760235677
openSNP	rs760235677
23andMe	rs760235677
SNPshot	rs760235677
SNPdbe	rs760235677
MSV3d	rs760235677
GWAS Ctlg	rs760235677

Max Magnitude

0

ClinVar
Risk	rs760235677(A;A) rs760235677(T;T)
Alt	rs760235677(A;A) rs760235677(T;T)
Reference	Rs760235677(G;G)
Significance	Other
Disease	Breast-ovarian cancer Hereditary cancer-predisposing syndrome Fanconi anemia not provided
Variation	info
Gene	RAD51C
CLNDBN	Breast-ovarian cancer, familial 3 Hereditary cancer-predisposing syndrome Fanconi anemia, complementation group O not provided
Reversed	0
HGVS	NC_000017.10:g.56787352G>A; NC_000017.10:g.56787352G>T
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000024267.2, RCV000221081.1, RCV000226369.2, RCV000409098.1, RCV000481912.1,