rs587782699

Orientation

plus

Stabilized

plus

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

Make rs587782699(-;TA)

Make rs587782699(TA;TA)

Reference

GRCh38.p2 38.2/144

Chromosome

17

Position

58696790

Gene

RAD51C

is a	snp
is	mentioned by
dbSNP	rs587782699
dbSNP (classic)	rs587782699
ClinGen	rs587782699
ebi	rs587782699
HLI	rs587782699
Exac	rs587782699
Gnomad	rs587782699
Varsome	rs587782699
LitVar	rs587782699
Map	rs587782699
PheGenI	rs587782699
Biobank	rs587782699
1000 genomes	rs587782699
hgdp	rs587782699
ensembl	rs587782699
geneview	rs587782699
scholar	rs587782699
google	rs587782699
pharmgkb	rs587782699
gwascentral	rs587782699
openSNP	rs587782699
23andMe	rs587782699
SNPshot	rs587782699
SNPdbe	rs587782699
MSV3d	rs587782699
GWAS Ctlg	rs587782699

Max Magnitude

0

ClinVar
Risk	rs587782699(AT;AT)
Alt	rs587782699(AT;AT)
Reference	Rs587782699(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	RAD51C
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000017.10:g.56774150_56774151dupTA
CLNSRC
CLNACC	RCV000132139.2,