rs63751411

Orientation

plus

Stabilized

plus

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

Make rs63751411(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47471041

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751411
dbSNP (classic)	rs63751411
ClinGen	rs63751411
ebi	rs63751411
HLI	rs63751411
Exac	rs63751411
Gnomad	rs63751411
Varsome	rs63751411
LitVar	rs63751411
Map	rs63751411
PheGenI	rs63751411
Biobank	rs63751411
1000 genomes	rs63751411
hgdp	rs63751411
ensembl	rs63751411
geneview	rs63751411
scholar	rs63751411
google	rs63751411
pharmgkb	rs63751411
gwascentral	rs63751411
openSNP	rs63751411
23andMe	rs63751411
SNPshot	rs63751411
SNPdbe	rs63751411
MSV3d	rs63751411
GWAS Ctlg	rs63751411

Max Magnitude

6

ClinVar
Risk	rs63751411(T;T)
Alt	rs63751411(T;T)
Reference	Rs63751411(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47698180G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076261.2, RCV000483706.1, RCV000491635.1,