rs587780129

Orientation

minus

Stabilized

minus

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

Make rs587780129(-;-)

Make rs587780129(-;A)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

152648940

Gene

XRCC2

is a	snp
is	mentioned by
dbSNP	rs587780129
dbSNP (classic)	rs587780129
ClinGen	rs587780129
ebi	rs587780129
HLI	rs587780129
Exac	rs587780129
Gnomad	rs587780129
Varsome	rs587780129
LitVar	rs587780129
Map	rs587780129
PheGenI	rs587780129
Biobank	rs587780129
1000 genomes	rs587780129
hgdp	rs587780129
ensembl	rs587780129
geneview	rs587780129
scholar	rs587780129
google	rs587780129
pharmgkb	rs587780129
gwascentral	rs587780129
openSNP	rs587780129
23andMe	rs587780129
SNPshot	rs587780129
SNPdbe	rs587780129
MSV3d	rs587780129
GWAS Ctlg	rs587780129

Max Magnitude

0

ClinVar
Risk	rs587780129(-;-)
Alt	rs587780129(-;-)
Reference	Rs587780129(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	XRCC2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000007.13:g.152346025delT
CLNSRC
CLNACC	RCV000115892.2,