rs587782528

Orientation

plus

Stabilized

plus

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

Make rs587782528(C;T)

Make rs587782528(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58692740

Gene	RAD51C, TEX14

is a	snp
is	mentioned by
dbSNP	rs587782528
dbSNP (classic)	rs587782528
ClinGen	rs587782528
ebi	rs587782528
HLI	rs587782528
Exac	rs587782528
Gnomad	rs587782528
Varsome	rs587782528
LitVar	rs587782528
Map	rs587782528
PheGenI	rs587782528
Biobank	rs587782528
1000 genomes	rs587782528
hgdp	rs587782528
ensembl	rs587782528
geneview	rs587782528
scholar	rs587782528
google	rs587782528
pharmgkb	rs587782528
gwascentral	rs587782528
openSNP	rs587782528
23andMe	rs587782528
SNPshot	rs587782528
SNPdbe	rs587782528
MSV3d	rs587782528
GWAS Ctlg	rs587782528

Max Magnitude

0

ClinVar
Risk	rs587782528(T;T)
Alt	rs587782528(T;T)
Reference	Rs587782528(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Fanconi anemia not provided Breast-ovarian cancer
Variation	info
Gene	TEX14 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.56770101C>T
CLNSRC
CLNACC	RCV000131716.4, RCV000196217.2, RCV000212932.1, RCV000410098.1,