rs63750896

Orientation

plus

Stabilized

plus

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

Make rs63750896(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478366

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750896
dbSNP (classic)	rs63750896
ClinGen	rs63750896
ebi	rs63750896
HLI	rs63750896
Exac	rs63750896
Gnomad	rs63750896
Varsome	rs63750896
LitVar	rs63750896
Map	rs63750896
PheGenI	rs63750896
Biobank	rs63750896
1000 genomes	rs63750896
hgdp	rs63750896
ensembl	rs63750896
geneview	rs63750896
scholar	rs63750896
google	rs63750896
pharmgkb	rs63750896
gwascentral	rs63750896
openSNP	rs63750896
23andMe	rs63750896
SNPshot	rs63750896
SNPdbe	rs63750896
MSV3d	rs63750896
GWAS Ctlg	rs63750896

Max Magnitude

6

ClinVar
Risk	rs63750896(-;-)
Alt	rs63750896(-;-)
Reference	Rs63750896(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47705505delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076456.2,