rs63751117

Orientation

plus

Stabilized

plus

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

Make rs63751117(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47480722

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751117
dbSNP (classic)	rs63751117
ClinGen	rs63751117
ebi	rs63751117
HLI	rs63751117
Exac	rs63751117
Gnomad	rs63751117
Varsome	rs63751117
LitVar	rs63751117
Map	rs63751117
PheGenI	rs63751117
Biobank	rs63751117
1000 genomes	rs63751117
hgdp	rs63751117
ensembl	rs63751117
geneview	rs63751117
scholar	rs63751117
google	rs63751117
pharmgkb	rs63751117
gwascentral	rs63751117
openSNP	rs63751117
23andMe	rs63751117
SNPshot	rs63751117
SNPdbe	rs63751117
MSV3d	rs63751117
GWAS Ctlg	rs63751117

Max Magnitude

6

ClinVar
Risk	rs63751117(-;-)
Alt	rs63751117(-;-)
Reference	Rs63751117(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707861delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076487.2,