rs63751169

Orientation

plus

Stabilized

plus

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

Make rs63751169(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429857

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751169
dbSNP (classic)	rs63751169
ClinGen	rs63751169
ebi	rs63751169
HLI	rs63751169
Exac	rs63751169
Gnomad	rs63751169
Varsome	rs63751169
LitVar	rs63751169
Map	rs63751169
PheGenI	rs63751169
Biobank	rs63751169
1000 genomes	rs63751169
hgdp	rs63751169
ensembl	rs63751169
geneview	rs63751169
scholar	rs63751169
google	rs63751169
pharmgkb	rs63751169
gwascentral	rs63751169
openSNP	rs63751169
23andMe	rs63751169
SNPshot	rs63751169
SNPdbe	rs63751169
MSV3d	rs63751169
GWAS Ctlg	rs63751169

Max Magnitude

6

ClinVar
Risk	rs63751169(G;G)
Alt	rs63751169(G;G)
Reference	Rs63751169(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47656996dupG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076057.2,