rs63751110

Orientation

plus

Stabilized

plus

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

Make rs63751110(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410322

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751110
dbSNP (classic)	rs63751110
ClinGen	rs63751110
ebi	rs63751110
HLI	rs63751110
Exac	rs63751110
Gnomad	rs63751110
Varsome	rs63751110
LitVar	rs63751110
Map	rs63751110
PheGenI	rs63751110
Biobank	rs63751110
1000 genomes	rs63751110
hgdp	rs63751110
ensembl	rs63751110
geneview	rs63751110
scholar	rs63751110
google	rs63751110
pharmgkb	rs63751110
gwascentral	rs63751110
openSNP	rs63751110
23andMe	rs63751110
SNPshot	rs63751110
SNPdbe	rs63751110
MSV3d	rs63751110
GWAS Ctlg	rs63751110

Max Magnitude

6

ClinVar
Risk	rs63751110(C;C)
Alt	rs63751110(C;C)
Reference	Rs63751110(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637461T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000076650.2,