rs587781490

Orientation

plus

Stabilized

plus

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

Make rs587781490(A;T)

Make rs587781490(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58696790

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587781490
dbSNP (classic)	rs587781490
ClinGen	rs587781490
ebi	rs587781490
HLI	rs587781490
Exac	rs587781490
Gnomad	rs587781490
Varsome	rs587781490
LitVar	rs587781490
Map	rs587781490
PheGenI	rs587781490
Biobank	rs587781490
1000 genomes	rs587781490
hgdp	rs587781490
ensembl	rs587781490
geneview	rs587781490
scholar	rs587781490
google	rs587781490
pharmgkb	rs587781490
gwascentral	rs587781490
openSNP	rs587781490
23andMe	rs587781490
SNPshot	rs587781490
SNPdbe	rs587781490
MSV3d	rs587781490
GWAS Ctlg	rs587781490

Max Magnitude

0

ClinVar
Risk	rs587781490(G;G) rs587781490(T;T)
Alt	rs587781490(G;G) rs587781490(T;T)
Reference	Rs587781490(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000017.10:g.56774151A>T
CLNSRC
CLNACC	RCV000129454.4, RCV000212939.1,