rs587779198

Orientation

plus

Stabilized

plus

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

Make rs587779198(G;G)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47416294

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779198
dbSNP (classic)	rs587779198
ClinGen	rs587779198
ebi	rs587779198
HLI	rs587779198
Exac	rs587779198
Gnomad	rs587779198
Varsome	rs587779198
LitVar	rs587779198
Map	rs587779198
PheGenI	rs587779198
Biobank	rs587779198
1000 genomes	rs587779198
hgdp	rs587779198
ensembl	rs587779198
geneview	rs587779198
scholar	rs587779198
google	rs587779198
pharmgkb	rs587779198
gwascentral	rs587779198
openSNP	rs587779198
23andMe	rs587779198
SNPshot	rs587779198
SNPdbe	rs587779198
MSV3d	rs587779198
GWAS Ctlg	rs587779198

Max Magnitude

6

ClinVar
Risk	rs587779198(G;G)
Alt	rs587779198(G;G)
Reference	Rs587779198(A;A)
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.47643433A>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076759.2, RCV000491601.1,