rs876658644

Orientation

plus

Stabilized

plus

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

Make rs876658644(A;A)

Make rs876658644(A;G)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

58703330

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs876658644
dbSNP (classic)	rs876658644
ClinGen	rs876658644
ebi	rs876658644
HLI	rs876658644
Exac	rs876658644
Gnomad	rs876658644
Varsome	rs876658644
LitVar	rs876658644
Map	rs876658644
PheGenI	rs876658644
Biobank	rs876658644
1000 genomes	rs876658644
hgdp	rs876658644
ensembl	rs876658644
geneview	rs876658644
scholar	rs876658644
google	rs876658644
pharmgkb	rs876658644
gwascentral	rs876658644
openSNP	rs876658644
23andMe	rs876658644
SNPshot	rs876658644
SNPdbe	rs876658644
MSV3d	rs876658644
GWAS Ctlg	rs876658644

Max Magnitude

0

ClinVar
Risk	rs876658644(A;A)
Alt	rs876658644(A;A)
Reference	Rs876658644(G;G)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56780691G>A
CLNSRC
CLNACC	RCV000218961.1,