rs63749802

Orientation

plus

Stabilized

plus

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

Make rs63749802(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476552

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749802
dbSNP (classic)	rs63749802
ClinGen	rs63749802
ebi	rs63749802
HLI	rs63749802
Exac	rs63749802
Gnomad	rs63749802
Varsome	rs63749802
LitVar	rs63749802
Map	rs63749802
PheGenI	rs63749802
Biobank	rs63749802
1000 genomes	rs63749802
hgdp	rs63749802
ensembl	rs63749802
geneview	rs63749802
scholar	rs63749802
google	rs63749802
pharmgkb	rs63749802
gwascentral	rs63749802
openSNP	rs63749802
23andMe	rs63749802
SNPshot	rs63749802
SNPdbe	rs63749802
MSV3d	rs63749802
GWAS Ctlg	rs63749802

Max Magnitude

6

ClinVar
Risk	rs63749802(T;T)
Alt	rs63749802(T;T)
Reference	Rs63749802(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703691G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076417.2,