rs587779138

Orientation

plus

Stabilized

plus

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

Make rs587779138(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47407923

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779138
dbSNP (classic)	rs587779138
ClinGen	rs587779138
ebi	rs587779138
HLI	rs587779138
Exac	rs587779138
Gnomad	rs587779138
Varsome	rs587779138
LitVar	rs587779138
Map	rs587779138
PheGenI	rs587779138
Biobank	rs587779138
1000 genomes	rs587779138
hgdp	rs587779138
ensembl	rs587779138
geneview	rs587779138
scholar	rs587779138
google	rs587779138
pharmgkb	rs587779138
gwascentral	rs587779138
openSNP	rs587779138
23andMe	rs587779138
SNPshot	rs587779138
SNPdbe	rs587779138
MSV3d	rs587779138
GWAS Ctlg	rs587779138

Max Magnitude

6

ClinVar
Risk	rs587779138(G;G)
Alt	rs587779138(G;G)
Reference	Rs587779138(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635062T>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076396.2,