rs63750872

Orientation

plus

Stabilized

plus

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

Make rs63750872(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476452

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750872
dbSNP (classic)	rs63750872
ClinGen	rs63750872
ebi	rs63750872
HLI	rs63750872
Exac	rs63750872
Gnomad	rs63750872
Varsome	rs63750872
LitVar	rs63750872
Map	rs63750872
PheGenI	rs63750872
Biobank	rs63750872
1000 genomes	rs63750872
hgdp	rs63750872
ensembl	rs63750872
geneview	rs63750872
scholar	rs63750872
google	rs63750872
pharmgkb	rs63750872
gwascentral	rs63750872
openSNP	rs63750872
23andMe	rs63750872
SNPshot	rs63750872
SNPdbe	rs63750872
MSV3d	rs63750872
GWAS Ctlg	rs63750872

Max Magnitude

6

ClinVar
Risk	rs63750872(A;A)
Alt	rs63750872(A;A)
Reference	Rs63750872(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703591T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076386.2,