rs63751158

Orientation

plus

Stabilized

plus

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

Make rs63751158(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47408444

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751158
dbSNP (classic)	rs63751158
ClinGen	rs63751158
ebi	rs63751158
HLI	rs63751158
Exac	rs63751158
Gnomad	rs63751158
Varsome	rs63751158
LitVar	rs63751158
Map	rs63751158
PheGenI	rs63751158
Biobank	rs63751158
1000 genomes	rs63751158
hgdp	rs63751158
ensembl	rs63751158
geneview	rs63751158
scholar	rs63751158
google	rs63751158
pharmgkb	rs63751158
gwascentral	rs63751158
openSNP	rs63751158
23andMe	rs63751158
SNPshot	rs63751158
SNPdbe	rs63751158
MSV3d	rs63751158
GWAS Ctlg	rs63751158

Max Magnitude

6

ClinVar
Risk	rs63751158(T;T)
Alt	rs63751158(T;T)
Reference	Rs63751158(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635583dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076504.2,