rs786202790

Orientation

plus

Stabilized

plus

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

Make rs786202790(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47475058

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs786202790
dbSNP (classic)	rs786202790
ClinGen	rs786202790
ebi	rs786202790
HLI	rs786202790
Exac	rs786202790
Gnomad	rs786202790
Varsome	rs786202790
LitVar	rs786202790
Map	rs786202790
PheGenI	rs786202790
Biobank	rs786202790
1000 genomes	rs786202790
hgdp	rs786202790
ensembl	rs786202790
geneview	rs786202790
scholar	rs786202790
google	rs786202790
pharmgkb	rs786202790
gwascentral	rs786202790
openSNP	rs786202790
23andMe	rs786202790
SNPshot	rs786202790
SNPdbe	rs786202790
MSV3d	rs786202790
GWAS Ctlg	rs786202790

Max Magnitude

6

ClinVar
Risk	rs786202790(-;-)
Alt	rs786202790(-;-)
Reference	Rs786202790(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47702197delT
CLNSRC
CLNACC	RCV000165778.1,