rs587779181

Orientation

plus

Stabilized

plus

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

Make rs587779181(CT;CT)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47412536

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs587779181
dbSNP (classic)	rs587779181
ClinGen	rs587779181
ebi	rs587779181
HLI	rs587779181
Exac	rs587779181
Gnomad	rs587779181
Varsome	rs587779181
LitVar	rs587779181
Map	rs587779181
PheGenI	rs587779181
Biobank	rs587779181
1000 genomes	rs587779181
hgdp	rs587779181
ensembl	rs587779181
geneview	rs587779181
scholar	rs587779181
google	rs587779181
pharmgkb	rs587779181
gwascentral	rs587779181
openSNP	rs587779181
23andMe	rs587779181
SNPshot	rs587779181
SNPdbe	rs587779181
MSV3d	rs587779181
GWAS Ctlg	rs587779181

Max Magnitude

6

ClinVar
Risk	rs587779181(CT;CT)
Alt	rs587779181(CT;CT)
Reference	Rs587779181(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639674_47639675dupCT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076706.2,