rs786201909

Orientation

plus

Stabilized

plus

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

Make rs786201909(G;G)

Make rs786201909(G;T)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

58703254

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs786201909
dbSNP (classic)	rs786201909
ClinGen	rs786201909
ebi	rs786201909
HLI	rs786201909
Exac	rs786201909
Gnomad	rs786201909
Varsome	rs786201909
LitVar	rs786201909
Map	rs786201909
PheGenI	rs786201909
Biobank	rs786201909
1000 genomes	rs786201909
hgdp	rs786201909
ensembl	rs786201909
geneview	rs786201909
scholar	rs786201909
google	rs786201909
pharmgkb	rs786201909
gwascentral	rs786201909
openSNP	rs786201909
23andMe	rs786201909
SNPshot	rs786201909
SNPdbe	rs786201909
MSV3d	rs786201909
GWAS Ctlg	rs786201909

Max Magnitude

0

ClinVar
Risk	rs786201909(G;G)
Alt	rs786201909(G;G)
Reference	Rs786201909(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56780615T>G
CLNSRC
CLNACC	RCV000164432.2,