rs587779121

Orientation

plus

Stabilized

plus

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

Make rs587779121(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47475249

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779121
dbSNP (classic)	rs587779121
ClinGen	rs587779121
ebi	rs587779121
HLI	rs587779121
Exac	rs587779121
Gnomad	rs587779121
Varsome	rs587779121
LitVar	rs587779121
Map	rs587779121
PheGenI	rs587779121
Biobank	rs587779121
1000 genomes	rs587779121
hgdp	rs587779121
ensembl	rs587779121
geneview	rs587779121
scholar	rs587779121
google	rs587779121
pharmgkb	rs587779121
gwascentral	rs587779121
openSNP	rs587779121
23andMe	rs587779121
SNPshot	rs587779121
SNPdbe	rs587779121
MSV3d	rs587779121
GWAS Ctlg	rs587779121

Max Magnitude

6

ClinVar
Risk	rs587779121(-;-)
Alt	rs587779121(-;-)
Reference	Rs587779121(AC;AC)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702388_47702389delCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076330.2,