rs587779191

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;GACT)	6	Lynch syndrome, pathogenic mutation
(ACTG;ACTG)	0	common in clinvar
(GACT;GACT)	0	common/normal

Make rs587779191(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47414349

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779191
dbSNP (classic)	rs587779191
ClinGen	rs587779191
ebi	rs587779191
HLI	rs587779191
Exac	rs587779191
Gnomad	rs587779191
Varsome	rs587779191
LitVar	rs587779191
Map	rs587779191
PheGenI	rs587779191
Biobank	rs587779191
1000 genomes	rs587779191
hgdp	rs587779191
ensembl	rs587779191
geneview	rs587779191
scholar	rs587779191
google	rs587779191
pharmgkb	rs587779191
gwascentral	rs587779191
openSNP	rs587779191
23andMe	rs587779191
SNPshot	rs587779191
SNPdbe	rs587779191
MSV3d	rs587779191
GWAS Ctlg	rs587779191

Max Magnitude

6

ClinVar
Risk	rs587779191(-;-)
Alt	rs587779191(-;-)
Reference	Rs587779191(ACTG;ACTG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641488_47641491delGACT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076741.2,