rs863225387

Orientation

plus

Stabilized

plus

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

Make rs863225387(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47429902

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs863225387
dbSNP (classic)	rs863225387
ClinGen	rs863225387
ebi	rs863225387
HLI	rs863225387
Exac	rs863225387
Gnomad	rs863225387
Varsome	rs863225387
LitVar	rs863225387
Map	rs863225387
PheGenI	rs863225387
Biobank	rs863225387
1000 genomes	rs863225387
hgdp	rs863225387
ensembl	rs863225387
geneview	rs863225387
scholar	rs863225387
google	rs863225387
pharmgkb	rs863225387
gwascentral	rs863225387
openSNP	rs863225387
23andMe	rs863225387
SNPshot	rs863225387
SNPdbe	rs863225387
MSV3d	rs863225387
GWAS Ctlg	rs863225387

Max Magnitude

0

ClinVar
Risk	rs863225387(T;T)
Alt	rs863225387(T;T)
Reference	Rs863225387(C;C)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47657041C>T
CLNSRC
CLNACC	RCV000202046.1, RCV000490844.1,