rs587781995

Orientation

plus

Stabilized

plus

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

Make rs587781995(-;-)

Make rs587781995(-;AG)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58724038

Gene	LOC105371843, RAD51C

is a	snp
is	mentioned by
dbSNP	rs587781995
dbSNP (classic)	rs587781995
ClinGen	rs587781995
ebi	rs587781995
HLI	rs587781995
Exac	rs587781995
Gnomad	rs587781995
Varsome	rs587781995
LitVar	rs587781995
Map	rs587781995
PheGenI	rs587781995
Biobank	rs587781995
1000 genomes	rs587781995
hgdp	rs587781995
ensembl	rs587781995
geneview	rs587781995
scholar	rs587781995
google	rs587781995
pharmgkb	rs587781995
gwascentral	rs587781995
openSNP	rs587781995
23andMe	rs587781995
SNPshot	rs587781995
SNPdbe	rs587781995
MSV3d	rs587781995
GWAS Ctlg	rs587781995

Max Magnitude

0

ClinVar
Risk	rs587781995(-;-)
Alt	rs587781995(-;-)
Reference	Rs587781995(AG;AG)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000017.10:g.56801399_56801400delAG
CLNSRC
CLNACC	RCV000130408.3, RCV000236611.2,