rs587779140

Orientation

plus

Stabilized

plus

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

Make rs587779140(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47476528

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779140
dbSNP (classic)	rs587779140
ClinGen	rs587779140
ebi	rs587779140
HLI	rs587779140
Exac	rs587779140
Gnomad	rs587779140
Varsome	rs587779140
LitVar	rs587779140
Map	rs587779140
PheGenI	rs587779140
Biobank	rs587779140
1000 genomes	rs587779140
hgdp	rs587779140
ensembl	rs587779140
geneview	rs587779140
scholar	rs587779140
google	rs587779140
pharmgkb	rs587779140
gwascentral	rs587779140
openSNP	rs587779140
23andMe	rs587779140
SNPshot	rs587779140
SNPdbe	rs587779140
MSV3d	rs587779140
GWAS Ctlg	rs587779140

Max Magnitude

6

ClinVar
Risk	rs587779140(T;T)
Alt	rs587779140(T;T)
Reference	Rs587779140(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703667dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076414.2,