rs63750521

Orientation

plus

Stabilized

plus

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

Make rs63750521(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47445644

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750521
dbSNP (classic)	rs63750521
ClinGen	rs63750521
ebi	rs63750521
HLI	rs63750521
Exac	rs63750521
Gnomad	rs63750521
Varsome	rs63750521
LitVar	rs63750521
Map	rs63750521
PheGenI	rs63750521
Biobank	rs63750521
1000 genomes	rs63750521
hgdp	rs63750521
ensembl	rs63750521
geneview	rs63750521
scholar	rs63750521
google	rs63750521
pharmgkb	rs63750521
gwascentral	rs63750521
openSNP	rs63750521
23andMe	rs63750521
SNPshot	rs63750521
SNPdbe	rs63750521
MSV3d	rs63750521
GWAS Ctlg	rs63750521

Max Magnitude

6

ClinVar
Risk	rs63750521(G;G)
Alt	rs63750521(G;G)
Reference	Rs63750521(T;T)
Significance	Pathogenic
Disease	Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47672783T>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076136.2, RCV000160582.1,