rs587779166

Orientation

plus

Stabilized

plus

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

Make rs587779166(A;A)

Make rs587779166(A;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47410319

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779166
dbSNP (classic)	rs587779166
ClinGen	rs587779166
ebi	rs587779166
HLI	rs587779166
Exac	rs587779166
Gnomad	rs587779166
Varsome	rs587779166
LitVar	rs587779166
Map	rs587779166
PheGenI	rs587779166
Biobank	rs587779166
1000 genomes	rs587779166
hgdp	rs587779166
ensembl	rs587779166
geneview	rs587779166
scholar	rs587779166
google	rs587779166
pharmgkb	rs587779166
gwascentral	rs587779166
openSNP	rs587779166
23andMe	rs587779166
SNPshot	rs587779166
SNPdbe	rs587779166
MSV3d	rs587779166
GWAS Ctlg	rs587779166

Max Magnitude

6

ClinVar
Risk	rs587779166(A;A) rs587779166(T;T)
Alt	rs587779166(A;A) rs587779166(T;T)
Reference	Rs587779166(G;G)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47637458G>A; NC_000002.11:g.47637458G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076647.2, RCV000491751.1,