rs587779189

Orientation

plus

Stabilized

plus

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

Make rs587779189(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47414339

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779189
dbSNP (classic)	rs587779189
ClinGen	rs587779189
ebi	rs587779189
HLI	rs587779189
Exac	rs587779189
Gnomad	rs587779189
Varsome	rs587779189
LitVar	rs587779189
Map	rs587779189
PheGenI	rs587779189
Biobank	rs587779189
1000 genomes	rs587779189
hgdp	rs587779189
ensembl	rs587779189
geneview	rs587779189
scholar	rs587779189
google	rs587779189
pharmgkb	rs587779189
gwascentral	rs587779189
openSNP	rs587779189
23andMe	rs587779189
SNPshot	rs587779189
SNPdbe	rs587779189
MSV3d	rs587779189
GWAS Ctlg	rs587779189

Max Magnitude

6

ClinVar
Risk	rs587779189(-;-)
Alt	rs587779189(-;-)
Reference	Rs587779189(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641478delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076739.2,