rs63750401

Orientation

plus

Stabilized

plus

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

Make rs63750401(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410143

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750401
dbSNP (classic)	rs63750401
ClinGen	rs63750401
ebi	rs63750401
HLI	rs63750401
Exac	rs63750401
Gnomad	rs63750401
Varsome	rs63750401
LitVar	rs63750401
Map	rs63750401
PheGenI	rs63750401
Biobank	rs63750401
1000 genomes	rs63750401
hgdp	rs63750401
ensembl	rs63750401
geneview	rs63750401
scholar	rs63750401
google	rs63750401
pharmgkb	rs63750401
gwascentral	rs63750401
openSNP	rs63750401
23andMe	rs63750401
SNPshot	rs63750401
SNPdbe	rs63750401
MSV3d	rs63750401
GWAS Ctlg	rs63750401

Max Magnitude

6

ClinVar
Risk	rs63750401(-;-)
Alt	rs63750401(-;-)
Reference	Rs63750401(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637282delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076597.2,