rs587779174

Orientation

plus

Stabilized

plus

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

Make rs587779174(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47412459

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779174
dbSNP (classic)	rs587779174
ClinGen	rs587779174
ebi	rs587779174
HLI	rs587779174
Exac	rs587779174
Gnomad	rs587779174
Varsome	rs587779174
LitVar	rs587779174
Map	rs587779174
PheGenI	rs587779174
Biobank	rs587779174
1000 genomes	rs587779174
hgdp	rs587779174
ensembl	rs587779174
geneview	rs587779174
scholar	rs587779174
google	rs587779174
pharmgkb	rs587779174
gwascentral	rs587779174
openSNP	rs587779174
23andMe	rs587779174
SNPshot	rs587779174
SNPdbe	rs587779174
MSV3d	rs587779174
GWAS Ctlg	rs587779174

Max Magnitude

6

ClinVar
Risk	rs587779174(-;-)
Alt	rs587779174(-;-)
Reference	Rs587779174(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639598delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076683.2,