rs267608000

Orientation

plus

Stabilized

plus

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

Make rs267608000(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476382

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs267608000
dbSNP (classic)	rs267608000
ClinGen	rs267608000
ebi	rs267608000
HLI	rs267608000
Exac	rs267608000
Gnomad	rs267608000
Varsome	rs267608000
LitVar	rs267608000
Map	rs267608000
PheGenI	rs267608000
Biobank	rs267608000
1000 genomes	rs267608000
hgdp	rs267608000
ensembl	rs267608000
geneview	rs267608000
scholar	rs267608000
google	rs267608000
pharmgkb	rs267608000
gwascentral	rs267608000
openSNP	rs267608000
23andMe	rs267608000
SNPshot	rs267608000
SNPdbe	rs267608000
MSV3d	rs267608000
GWAS Ctlg	rs267608000

Max Magnitude

6

ClinVar
Risk	rs267608000(-;-)
Alt	rs267608000(-;-)
Reference	Rs267608000(GT;GT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703521_47703522delGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076364.2,