rs63750039

Orientation

plus

Stabilized

plus

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

Make rs63750039(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429804

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750039
dbSNP (classic)	rs63750039
ClinGen	rs63750039
ebi	rs63750039
HLI	rs63750039
Exac	rs63750039
Gnomad	rs63750039
Varsome	rs63750039
LitVar	rs63750039
Map	rs63750039
PheGenI	rs63750039
Biobank	rs63750039
1000 genomes	rs63750039
hgdp	rs63750039
ensembl	rs63750039
geneview	rs63750039
scholar	rs63750039
google	rs63750039
pharmgkb	rs63750039
gwascentral	rs63750039
openSNP	rs63750039
23andMe	rs63750039
SNPshot	rs63750039
SNPdbe	rs63750039
MSV3d	rs63750039
GWAS Ctlg	rs63750039

Max Magnitude

6

ClinVar
Risk	rs63750039(-;-)
Alt	rs63750039(-;-)
Reference	Rs63750039(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47656943delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076046.2,