rs587779083

Orientation

plus

Stabilized

plus

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

Make rs587779083(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47445589

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779083
dbSNP (classic)	rs587779083
ClinGen	rs587779083
ebi	rs587779083
HLI	rs587779083
Exac	rs587779083
Gnomad	rs587779083
Varsome	rs587779083
LitVar	rs587779083
Map	rs587779083
PheGenI	rs587779083
Biobank	rs587779083
1000 genomes	rs587779083
hgdp	rs587779083
ensembl	rs587779083
geneview	rs587779083
scholar	rs587779083
google	rs587779083
pharmgkb	rs587779083
gwascentral	rs587779083
openSNP	rs587779083
23andMe	rs587779083
SNPshot	rs587779083
SNPdbe	rs587779083
MSV3d	rs587779083
GWAS Ctlg	rs587779083

Max Magnitude

6

ClinVar
Risk	rs587779083(-;-)
Alt	rs587779083(-;-)
Reference	Rs587779083(CT;CT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47672728_47672729delCT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076120.2,