rs869312804

Merged into

rs730882048

Orientation

minus

Stabilized

minus

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

Make rs869312804(-;-)

Make rs869312804(-;T)

Reference

GRCh38.p7 38.3/149

Chromosome

7

Position

152660727

Gene

XRCC2

is a	snp
is	mentioned by
dbSNP	rs869312804
dbSNP (classic)	rs869312804
ClinGen	rs869312804
ebi	rs869312804
HLI	rs869312804
Exac	rs869312804
Gnomad	rs869312804
Varsome	rs869312804
LitVar	rs869312804
Map	rs869312804
PheGenI	rs869312804
Biobank	rs869312804
1000 genomes	rs869312804
hgdp	rs869312804
ensembl	rs869312804
geneview	rs869312804
scholar	rs869312804
google	rs869312804
pharmgkb	rs869312804
gwascentral	rs869312804
openSNP	rs869312804
23andMe	rs869312804
SNPshot	rs869312804
SNPdbe	rs869312804
MSV3d	rs869312804
GWAS Ctlg	rs869312804

Status

Merged into rs730882048

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs869312804(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	XRCC2
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	1
HGVS	NC_000007.13:g.152357811delA
CLNSRC
CLNACC	RCV000161115.2, RCV000254696.1,