rs786203036

Orientation

plus

Stabilized

plus

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

Make rs786203036(G;G)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47463086

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786203036
dbSNP (classic)	rs786203036
ClinGen	rs786203036
ebi	rs786203036
HLI	rs786203036
Exac	rs786203036
Gnomad	rs786203036
Varsome	rs786203036
LitVar	rs786203036
Map	rs786203036
PheGenI	rs786203036
Biobank	rs786203036
1000 genomes	rs786203036
hgdp	rs786203036
ensembl	rs786203036
geneview	rs786203036
scholar	rs786203036
google	rs786203036
pharmgkb	rs786203036
gwascentral	rs786203036
openSNP	rs786203036
23andMe	rs786203036
SNPshot	rs786203036
SNPdbe	rs786203036
MSV3d	rs786203036
GWAS Ctlg	rs786203036

Max Magnitude

6

ClinVar
Risk	rs786203036(A;A) rs786203036(G;G)
Alt	rs786203036(A;A) rs786203036(G;G)
Reference	Rs786203036(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47690225T>A; NC_000002.11:g.47690225T>G
CLNSRC
CLNACC	RCV000168254.1, RCV000166169.1,