rs587779197

Orientation

plus

Stabilized

plus

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

Make rs587779197(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47414418

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779197
dbSNP (classic)	rs587779197
ClinGen	rs587779197
ebi	rs587779197
HLI	rs587779197
Exac	rs587779197
Gnomad	rs587779197
Varsome	rs587779197
LitVar	rs587779197
Map	rs587779197
PheGenI	rs587779197
Biobank	rs587779197
1000 genomes	rs587779197
hgdp	rs587779197
ensembl	rs587779197
geneview	rs587779197
scholar	rs587779197
google	rs587779197
pharmgkb	rs587779197
gwascentral	rs587779197
openSNP	rs587779197
23andMe	rs587779197
SNPshot	rs587779197
SNPdbe	rs587779197
MSV3d	rs587779197
GWAS Ctlg	rs587779197

Max Magnitude

6

ClinVar
Risk	rs587779197(A;A)
Alt	rs587779197(A;A)
Reference	Rs587779197(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641557G>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076756.2,