rs730881941

Orientation

plus

Stabilized

plus

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

Make rs730881941(-;-)

Make rs730881941(-;CAGGG)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58724037

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs730881941
dbSNP (classic)	rs730881941
ClinGen	rs730881941
ebi	rs730881941
HLI	rs730881941
Exac	rs730881941
Gnomad	rs730881941
Varsome	rs730881941
LitVar	rs730881941
Map	rs730881941
PheGenI	rs730881941
Biobank	rs730881941
1000 genomes	rs730881941
hgdp	rs730881941
ensembl	rs730881941
geneview	rs730881941
scholar	rs730881941
google	rs730881941
pharmgkb	rs730881941
gwascentral	rs730881941
openSNP	rs730881941
23andMe	rs730881941
SNPshot	rs730881941
SNPdbe	rs730881941
MSV3d	rs730881941
GWAS Ctlg	rs730881941

Max Magnitude

0

ClinVar
Risk	rs730881941(-;-)
Alt	rs730881941(-;-)
Reference	Rs730881941(CAGGG;CAGGG)
Significance	Pathogenic
Disease	not provided
Variation	info
Gene	RAD51C
CLNDBN	not provided
Reversed	0
HGVS	NC_000017.10:g.56801398_56801402delCAGGG
CLNSRC
CLNACC	RCV000160935.2,