rs63750495

Orientation

plus

Stabilized

plus

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

Make rs63750495(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47475053

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750495
dbSNP (classic)	rs63750495
ClinGen	rs63750495
ebi	rs63750495
HLI	rs63750495
Exac	rs63750495
Gnomad	rs63750495
Varsome	rs63750495
LitVar	rs63750495
Map	rs63750495
PheGenI	rs63750495
Biobank	rs63750495
1000 genomes	rs63750495
hgdp	rs63750495
ensembl	rs63750495
geneview	rs63750495
scholar	rs63750495
google	rs63750495
pharmgkb	rs63750495
gwascentral	rs63750495
openSNP	rs63750495
23andMe	rs63750495
SNPshot	rs63750495
SNPdbe	rs63750495
MSV3d	rs63750495
GWAS Ctlg	rs63750495

Max Magnitude

6

ClinVar
Risk	rs63750495(-;-)
Alt	rs63750495(-;-)
Reference	Rs63750495(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702192_47702193delTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076288.2,