rs587779149

Orientation

plus

Stabilized

plus

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

Make rs587779149(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47480782

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779149
dbSNP (classic)	rs587779149
ClinGen	rs587779149
ebi	rs587779149
HLI	rs587779149
Exac	rs587779149
Gnomad	rs587779149
Varsome	rs587779149
LitVar	rs587779149
Map	rs587779149
PheGenI	rs587779149
Biobank	rs587779149
1000 genomes	rs587779149
hgdp	rs587779149
ensembl	rs587779149
geneview	rs587779149
scholar	rs587779149
google	rs587779149
pharmgkb	rs587779149
gwascentral	rs587779149
openSNP	rs587779149
23andMe	rs587779149
SNPshot	rs587779149
SNPdbe	rs587779149
MSV3d	rs587779149
GWAS Ctlg	rs587779149

Max Magnitude

6

ClinVar
Risk	rs587779149(-;-)
Alt	rs587779149(-;-)
Reference	Rs587779149(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707921delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076499.2,