rs63750091

Orientation

plus

Stabilized

plus

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

Make rs63750091(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414315

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750091
dbSNP (classic)	rs63750091
ClinGen	rs63750091
ebi	rs63750091
HLI	rs63750091
Exac	rs63750091
Gnomad	rs63750091
Varsome	rs63750091
LitVar	rs63750091
Map	rs63750091
PheGenI	rs63750091
Biobank	rs63750091
1000 genomes	rs63750091
hgdp	rs63750091
ensembl	rs63750091
geneview	rs63750091
scholar	rs63750091
google	rs63750091
pharmgkb	rs63750091
gwascentral	rs63750091
openSNP	rs63750091
23andMe	rs63750091
SNPshot	rs63750091
SNPdbe	rs63750091
MSV3d	rs63750091
GWAS Ctlg	rs63750091

Max Magnitude

6

ClinVar
Risk	rs63750091(T;T)
Alt	rs63750091(T;T)
Reference	Rs63750091(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641454dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076733.2,