rs63751140

Orientation

plus

Stabilized

plus

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

Make rs63751140(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47471062

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751140
dbSNP (classic)	rs63751140
ClinGen	rs63751140
ebi	rs63751140
HLI	rs63751140
Exac	rs63751140
Gnomad	rs63751140
Varsome	rs63751140
LitVar	rs63751140
Map	rs63751140
PheGenI	rs63751140
Biobank	rs63751140
1000 genomes	rs63751140
hgdp	rs63751140
ensembl	rs63751140
geneview	rs63751140
scholar	rs63751140
google	rs63751140
pharmgkb	rs63751140
gwascentral	rs63751140
openSNP	rs63751140
23andMe	rs63751140
SNPshot	rs63751140
SNPdbe	rs63751140
MSV3d	rs63751140
GWAS Ctlg	rs63751140

Max Magnitude

6

ClinVar
Risk	rs63751140(C;C) rs63751140(T;T)
Alt	rs63751140(C;C) rs63751140(T;T)
Reference	Rs63751140(G;G)
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.47698201G>C; NC_000002.11:g.47698201G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076270.2, RCV000491233.1,