rs587779112

Orientation

plus

Stabilized

plus

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

Make rs587779112(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47475092

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779112
dbSNP (classic)	rs587779112
ClinGen	rs587779112
ebi	rs587779112
HLI	rs587779112
Exac	rs587779112
Gnomad	rs587779112
Varsome	rs587779112
LitVar	rs587779112
Map	rs587779112
PheGenI	rs587779112
Biobank	rs587779112
1000 genomes	rs587779112
hgdp	rs587779112
ensembl	rs587779112
geneview	rs587779112
scholar	rs587779112
google	rs587779112
pharmgkb	rs587779112
gwascentral	rs587779112
openSNP	rs587779112
23andMe	rs587779112
SNPshot	rs587779112
SNPdbe	rs587779112
MSV3d	rs587779112
GWAS Ctlg	rs587779112

Max Magnitude

6

ClinVar
Risk	rs587779112(-;-)
Alt	rs587779112(-;-)
Reference	Rs587779112(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.47702231delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076297.2, RCV000491249.1,