rs143153871

Orientation

plus

Stabilized

plus

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

Make rs143153871(A;A)

Make rs143153871(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

7

Position

152648842

Gene

XRCC2

is a	snp
is	mentioned by
dbSNP	rs143153871
dbSNP (classic)	rs143153871
ClinGen	rs143153871
ebi	rs143153871
HLI	rs143153871
Exac	rs143153871
Gnomad	rs143153871
Varsome	rs143153871
LitVar	rs143153871
Map	rs143153871
PheGenI	rs143153871
Biobank	rs143153871
1000 genomes	rs143153871
hgdp	rs143153871
ensembl	rs143153871
geneview	rs143153871
scholar	rs143153871
google	rs143153871
pharmgkb	rs143153871
gwascentral	rs143153871
openSNP	rs143153871
23andMe	rs143153871
SNPshot	rs143153871
SNPdbe	rs143153871
MSV3d	rs143153871
GWAS Ctlg	rs143153871

Max Magnitude

0

ClinVar
Risk	rs143153871(A;A)
Alt	rs143153871(A;A)
Reference	Rs143153871(G;G)
Significance	Pathogenic
Disease	Variant of unknown significance Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	XRCC2
CLNDBN	Variant of unknown significance Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000007.13:g.152345927G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000022966.5, RCV000210083.1, RCV000236424.1,