rs587779176

Orientation

plus

Stabilized

plus

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

Make rs587779176(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47412493

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779176
dbSNP (classic)	rs587779176
ClinGen	rs587779176
ebi	rs587779176
HLI	rs587779176
Exac	rs587779176
Gnomad	rs587779176
Varsome	rs587779176
LitVar	rs587779176
Map	rs587779176
PheGenI	rs587779176
Biobank	rs587779176
1000 genomes	rs587779176
hgdp	rs587779176
ensembl	rs587779176
geneview	rs587779176
scholar	rs587779176
google	rs587779176
pharmgkb	rs587779176
gwascentral	rs587779176
openSNP	rs587779176
23andMe	rs587779176
SNPshot	rs587779176
SNPdbe	rs587779176
MSV3d	rs587779176
GWAS Ctlg	rs587779176

Max Magnitude

6

ClinVar
Risk	rs587779176(A;A)
Alt	rs587779176(A;A)
Reference	Rs587779176(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639632dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076692.2,