rs63749872

Orientation

plus

Stabilized

plus

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

Make rs63749872(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47408467

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749872
dbSNP (classic)	rs63749872
ClinGen	rs63749872
ebi	rs63749872
HLI	rs63749872
Exac	rs63749872
Gnomad	rs63749872
Varsome	rs63749872
LitVar	rs63749872
Map	rs63749872
PheGenI	rs63749872
Biobank	rs63749872
1000 genomes	rs63749872
hgdp	rs63749872
ensembl	rs63749872
geneview	rs63749872
scholar	rs63749872
google	rs63749872
pharmgkb	rs63749872
gwascentral	rs63749872
openSNP	rs63749872
23andMe	rs63749872
SNPshot	rs63749872
SNPdbe	rs63749872
MSV3d	rs63749872
GWAS Ctlg	rs63749872

Max Magnitude

6

ClinVar
Risk	rs63749872(-;-)
Alt	rs63749872(-;-)
Reference	Rs63749872(TT;TT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635606_47635607delTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076548.2,