rs587779145

Orientation

plus

Stabilized

plus

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

Make rs587779145(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47408433

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779145
dbSNP (classic)	rs587779145
ClinGen	rs587779145
ebi	rs587779145
HLI	rs587779145
Exac	rs587779145
Gnomad	rs587779145
Varsome	rs587779145
LitVar	rs587779145
Map	rs587779145
PheGenI	rs587779145
Biobank	rs587779145
1000 genomes	rs587779145
hgdp	rs587779145
ensembl	rs587779145
geneview	rs587779145
scholar	rs587779145
google	rs587779145
pharmgkb	rs587779145
gwascentral	rs587779145
openSNP	rs587779145
23andMe	rs587779145
SNPshot	rs587779145
SNPdbe	rs587779145
MSV3d	rs587779145
GWAS Ctlg	rs587779145

Max Magnitude

6

ClinVar
Risk	rs587779145(T;T)
Alt	rs587779145(T;T)
Reference	Rs587779145(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635572A>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076477.2,