rs863225395

Orientation

plus

Stabilized

plus

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

Make rs863225395(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47478361

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs863225395
dbSNP (classic)	rs863225395
ClinGen	rs863225395
ebi	rs863225395
HLI	rs863225395
Exac	rs863225395
Gnomad	rs863225395
Varsome	rs863225395
LitVar	rs863225395
Map	rs863225395
PheGenI	rs863225395
Biobank	rs863225395
1000 genomes	rs863225395
hgdp	rs863225395
ensembl	rs863225395
geneview	rs863225395
scholar	rs863225395
google	rs863225395
pharmgkb	rs863225395
gwascentral	rs863225395
openSNP	rs863225395
23andMe	rs863225395
SNPshot	rs863225395
SNPdbe	rs863225395
MSV3d	rs863225395
GWAS Ctlg	rs863225395

Max Magnitude

6

ClinVar
Risk	rs863225395(G;G)
Alt	rs863225395(G;G)
Reference	Rs863225395(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.47705500C>G
CLNSRC
CLNACC	RCV000202080.1, RCV000491337.1,