rs587779073

Orientation

plus

Stabilized

plus

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

Make rs587779073(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47429764

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779073
dbSNP (classic)	rs587779073
ClinGen	rs587779073
ebi	rs587779073
HLI	rs587779073
Exac	rs587779073
Gnomad	rs587779073
Varsome	rs587779073
LitVar	rs587779073
Map	rs587779073
PheGenI	rs587779073
Biobank	rs587779073
1000 genomes	rs587779073
hgdp	rs587779073
ensembl	rs587779073
geneview	rs587779073
scholar	rs587779073
google	rs587779073
pharmgkb	rs587779073
gwascentral	rs587779073
openSNP	rs587779073
23andMe	rs587779073
SNPshot	rs587779073
SNPdbe	rs587779073
MSV3d	rs587779073
GWAS Ctlg	rs587779073

Max Magnitude

6

ClinVar
Risk	rs587779073(-;-)
Alt	rs587779073(-;-)
Reference	Rs587779073(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47656903delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076039.2,