rs63751161

Orientation

plus

Stabilized

plus

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

Make rs63751161(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476376

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751161
dbSNP (classic)	rs63751161
ClinGen	rs63751161
ebi	rs63751161
HLI	rs63751161
Exac	rs63751161
Gnomad	rs63751161
Varsome	rs63751161
LitVar	rs63751161
Map	rs63751161
PheGenI	rs63751161
Biobank	rs63751161
1000 genomes	rs63751161
hgdp	rs63751161
ensembl	rs63751161
geneview	rs63751161
scholar	rs63751161
google	rs63751161
pharmgkb	rs63751161
gwascentral	rs63751161
openSNP	rs63751161
23andMe	rs63751161
SNPshot	rs63751161
SNPdbe	rs63751161
MSV3d	rs63751161
GWAS Ctlg	rs63751161

Max Magnitude

6

ClinVar
Risk	rs63751161(-;-)
Alt	rs63751161(-;-)
Reference	Rs63751161(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703515delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076361.2,