rs786202563

Orientation

plus

Stabilized

plus

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

Make rs786202563(-;-)

Make rs786202563(-;ACCAA)

Make rs786202563(ACCAA;ACCAA)

Reference

GRCh38.p2 38.2/146

Chromosome

17

Position

58695001

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs786202563
dbSNP (classic)	rs786202563
ClinGen	rs786202563
ebi	rs786202563
HLI	rs786202563
Exac	rs786202563
Gnomad	rs786202563
Varsome	rs786202563
LitVar	rs786202563
Map	rs786202563
PheGenI	rs786202563
Biobank	rs786202563
1000 genomes	rs786202563
hgdp	rs786202563
ensembl	rs786202563
geneview	rs786202563
scholar	rs786202563
google	rs786202563
pharmgkb	rs786202563
gwascentral	rs786202563
openSNP	rs786202563
23andMe	rs786202563
SNPshot	rs786202563
SNPdbe	rs786202563
MSV3d	rs786202563
GWAS Ctlg	rs786202563

Max Magnitude

0

ClinVar
Risk	rs786202563(-;-)
Alt	rs786202563(-;-)
Reference	Rs786202563(AAACC;AAACC)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56772362_56772366delACCAA
CLNSRC
CLNACC	RCV000165425.1,