rs63751133

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GT)	6	Lynch syndrome, pathogenic mutation
(GT;GT)	0	common in clinvar
(TG;TG)	0	common in clinvar

Make rs63751133(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414286

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751133
dbSNP (classic)	rs63751133
ClinGen	rs63751133
ebi	rs63751133
HLI	rs63751133
Exac	rs63751133
Gnomad	rs63751133
Varsome	rs63751133
LitVar	rs63751133
Map	rs63751133
PheGenI	rs63751133
Biobank	rs63751133
1000 genomes	rs63751133
hgdp	rs63751133
ensembl	rs63751133
geneview	rs63751133
scholar	rs63751133
google	rs63751133
pharmgkb	rs63751133
gwascentral	rs63751133
openSNP	rs63751133
23andMe	rs63751133
SNPshot	rs63751133
SNPdbe	rs63751133
MSV3d	rs63751133
GWAS Ctlg	rs63751133

Max Magnitude

6

ClinVar
Risk	rs63751133(-;-)
Alt	rs63751133(-;-)
Reference	Rs63751133(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641425_47641426delGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076725.2,