rs63751668

Orientation

plus

Stabilized

plus

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

Make rs63751668(A;A)

Make rs63751668(A;G)

Reference

GRCh38 38.1/142

Chromosome

2

Position

47475270

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751668
dbSNP (classic)	rs63751668
ClinGen	rs63751668
ebi	rs63751668
HLI	rs63751668
Exac	rs63751668
Gnomad	rs63751668
Varsome	rs63751668
LitVar	rs63751668
Map	rs63751668
PheGenI	rs63751668
Biobank	rs63751668
1000 genomes	rs63751668
hgdp	rs63751668
ensembl	rs63751668
geneview	rs63751668
scholar	rs63751668
google	rs63751668
pharmgkb	rs63751668
gwascentral	rs63751668
openSNP	rs63751668
23andMe	rs63751668
SNPshot	rs63751668
SNPdbe	rs63751668
MSV3d	rs63751668
GWAS Ctlg	rs63751668

Max Magnitude

6

ClinVar
Risk	rs63751668(A;A) rs63751668(C;C)
Alt	rs63751668(A;A) rs63751668(C;C)
Reference	Rs63751668(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702409G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076346.2,