rs2303425

Orientation

plus

Stabilized

plus

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

Make rs2303425(C;C)

Make rs2303425(C;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403074

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs2303425
dbSNP (classic)	rs2303425
ClinGen	rs2303425
ebi	rs2303425
HLI	rs2303425
Exac	rs2303425
Gnomad	rs2303425
Varsome	rs2303425
LitVar	rs2303425
Map	rs2303425
PheGenI	rs2303425
Biobank	rs2303425
1000 genomes	rs2303425
hgdp	rs2303425
ensembl	rs2303425
geneview	rs2303425
scholar	rs2303425
google	rs2303425
pharmgkb	rs2303425
gwascentral	rs2303425
openSNP	rs2303425
23andMe	rs2303425
SNPshot	rs2303425
SNPdbe	rs2303425
MSV3d	rs2303425
GWAS Ctlg	rs2303425

Max Magnitude

0

[PMID 25252909] Mismatch Repair Gene Polymorphisms and Association with Lung Cancer Development

ClinVar
Risk	rs2303425(C;C)
Alt	rs2303425(C;C)
Reference	Rs2303425(T;T)
Significance	Non-pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not specified
Reversed	0
HGVS	NC_000002.11:g.47630213T>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000075980.3, RCV000162385.1, RCV000253946.1,

[PMID 26975740] MSH2 rs2303425 Polymorphism is Associated with Early-Onset Breast Cancer in Taiwan.