rs2303426

Orientation

plus

Stabilized

plus

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

Make rs2303426(C;G)

Make rs2303426(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403411

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs2303426
dbSNP (classic)	rs2303426
ClinGen	rs2303426
ebi	rs2303426
HLI	rs2303426
Exac	rs2303426
Gnomad	rs2303426
Varsome	rs2303426
LitVar	rs2303426
Map	rs2303426
PheGenI	rs2303426
Biobank	rs2303426
1000 genomes	rs2303426
hgdp	rs2303426
ensembl	rs2303426
geneview	rs2303426
scholar	rs2303426
google	rs2303426
pharmgkb	rs2303426
gwascentral	rs2303426
openSNP	rs2303426
23andMe	rs2303426
SNPshot	rs2303426
SNPdbe	rs2303426
MSV3d	rs2303426
GWAS Ctlg	rs2303426

GMAF

0.3843

Max Magnitude

0

[PMID 21283657] Gallbladder Cancer Predisposition: A Multigenic Approach to DNA-Repair, Apoptotic and Inflammatory Pathway Genes

ClinVar
Risk	rs2303426(A;A) rs2303426(G;G)
Alt	rs2303426(A;A) rs2303426(G;G)
Reference	Rs2303426(C;C)
Significance	Probable-non-pathogenic
Disease	Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not specified Lynch syndrome I Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47630550C>A; NC_000002.11:g.47630550C>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000230066.1, RCV000030249.4, RCV000035360.9, RCV000144620.1, RCV000448740.1,

[PMID 20564624] Polymorphisms in ERCC2, MSH2, and OGG1 DNA repair genes and gallbladder cancer risk in a population of Northern India.