rs730882048

Orientation

minus

Stabilized

minus

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

Make rs730882048(-;-)

Make rs730882048(-;T)

Reference

GRCh38.p2 38.2/144

Chromosome

7

Position

152660726

Gene

XRCC2

is a	snp
is	mentioned by
dbSNP	rs730882048
dbSNP (classic)	rs730882048
ClinGen	rs730882048
ebi	rs730882048
HLI	rs730882048
Exac	rs730882048
Gnomad	rs730882048
Varsome	rs730882048
LitVar	rs730882048
Map	rs730882048
PheGenI	rs730882048
Biobank	rs730882048
1000 genomes	rs730882048
hgdp	rs730882048
ensembl	rs730882048
geneview	rs730882048
scholar	rs730882048
google	rs730882048
pharmgkb	rs730882048
gwascentral	rs730882048
openSNP	rs730882048
23andMe	rs730882048
SNPshot	rs730882048
SNPdbe	rs730882048
MSV3d	rs730882048
GWAS Ctlg	rs730882048

Merged from

Rs869312804

Max Magnitude

0

ClinVar
Risk	rs730882048(-;-)
Alt	rs730882048(-;-)
Reference	Rs730882048(T;T)
Significance	Probable-Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided not specified
Variation	info
Gene	XRCC2
CLNDBN	Hereditary cancer-predisposing syndrome not provided not specified
Reversed	1
HGVS	NC_000007.13:g.152357811delA
CLNSRC
CLNACC	RCV000161115.2, RCV000254696.2, RCV000471868.1,