rs63750302

Orientation

plus

Stabilized

plus

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

Make rs63750302(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429848

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750302
dbSNP (classic)	rs63750302
ClinGen	rs63750302
ebi	rs63750302
HLI	rs63750302
Exac	rs63750302
Gnomad	rs63750302
Varsome	rs63750302
LitVar	rs63750302
Map	rs63750302
PheGenI	rs63750302
Biobank	rs63750302
1000 genomes	rs63750302
hgdp	rs63750302
ensembl	rs63750302
geneview	rs63750302
scholar	rs63750302
google	rs63750302
pharmgkb	rs63750302
gwascentral	rs63750302
openSNP	rs63750302
23andMe	rs63750302
SNPshot	rs63750302
SNPdbe	rs63750302
MSV3d	rs63750302
GWAS Ctlg	rs63750302

Max Magnitude

6

ClinVar
Risk	rs63750302(T;T)
Alt	rs63750302(T;T)
Reference	Rs63750302(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47656987C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076054.2,