rs63750362

Orientation

plus

Stabilized

plus

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

Make rs63750362(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47463138

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750362
dbSNP (classic)	rs63750362
ClinGen	rs63750362
ebi	rs63750362
HLI	rs63750362
Exac	rs63750362
Gnomad	rs63750362
Varsome	rs63750362
LitVar	rs63750362
Map	rs63750362
PheGenI	rs63750362
Biobank	rs63750362
1000 genomes	rs63750362
hgdp	rs63750362
ensembl	rs63750362
geneview	rs63750362
scholar	rs63750362
google	rs63750362
pharmgkb	rs63750362
gwascentral	rs63750362
openSNP	rs63750362
23andMe	rs63750362
SNPshot	rs63750362
SNPdbe	rs63750362
MSV3d	rs63750362
GWAS Ctlg	rs63750362

Max Magnitude

6

ClinVar
Risk	rs63750362(T;T)
Alt	rs63750362(T;T)
Reference	Rs63750362(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690277dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076176.2,