rs763872353

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;T)	6	Lynch syndrome
(T;T)	0	common in clinvar

Make rs763872353(C;C)

Make rs763872353(C;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47408483

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs763872353
dbSNP (classic)	rs763872353
ClinGen	rs763872353
ebi	rs763872353
HLI	rs763872353
Exac	rs763872353
Gnomad	rs763872353
Varsome	rs763872353
LitVar	rs763872353
Map	rs763872353
PheGenI	rs763872353
Biobank	rs763872353
1000 genomes	rs763872353
hgdp	rs763872353
ensembl	rs763872353
geneview	rs763872353
scholar	rs763872353
google	rs763872353
pharmgkb	rs763872353
gwascentral	rs763872353
openSNP	rs763872353
23andMe	rs763872353
SNPshot	rs763872353
SNPdbe	rs763872353
MSV3d	rs763872353
GWAS Ctlg	rs763872353

Max Magnitude

6

ClinVar
Risk	rs763872353(A;A) rs763872353(C;C)
Alt	rs763872353(A;A) rs763872353(C;C)
Reference	Rs763872353(T;T)
Significance	Probable-Pathogenic
Disease	not provided
Variation	info
Gene	MSH2
CLNDBN	not provided
Reversed	0
HGVS	NC_000002.11:g.47635622T>A
CLNSRC
CLNACC	RCV000235827.1,