rs876659497

Orientation

plus

Stabilized

plus

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

Make rs876659497(-;-)

Make rs876659497(-;AT)

Reference

GRCh38.p2 38.2/147

Chromosome

17

Position

58703246

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs876659497
dbSNP (classic)	rs876659497
ClinGen	rs876659497
ebi	rs876659497
HLI	rs876659497
Exac	rs876659497
Gnomad	rs876659497
Varsome	rs876659497
LitVar	rs876659497
Map	rs876659497
PheGenI	rs876659497
Biobank	rs876659497
1000 genomes	rs876659497
hgdp	rs876659497
ensembl	rs876659497
geneview	rs876659497
scholar	rs876659497
google	rs876659497
pharmgkb	rs876659497
gwascentral	rs876659497
openSNP	rs876659497
23andMe	rs876659497
SNPshot	rs876659497
SNPdbe	rs876659497
MSV3d	rs876659497
GWAS Ctlg	rs876659497

Max Magnitude

0

ClinVar
Risk	rs876659497(-;-)
Alt	rs876659497(-;-)
Reference	Rs876659497(AT;AT)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56780607_56780608delAT
CLNSRC
CLNACC	RCV000214716.1,