rs63751160

Orientation

plus

Stabilized

plus

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

Make rs63751160(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47412527

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751160
dbSNP (classic)	rs63751160
ClinGen	rs63751160
ebi	rs63751160
HLI	rs63751160
Exac	rs63751160
Gnomad	rs63751160
Varsome	rs63751160
LitVar	rs63751160
Map	rs63751160
PheGenI	rs63751160
Biobank	rs63751160
1000 genomes	rs63751160
hgdp	rs63751160
ensembl	rs63751160
geneview	rs63751160
scholar	rs63751160
google	rs63751160
pharmgkb	rs63751160
gwascentral	rs63751160
openSNP	rs63751160
23andMe	rs63751160
SNPshot	rs63751160
SNPdbe	rs63751160
MSV3d	rs63751160
GWAS Ctlg	rs63751160

Max Magnitude

6

ClinVar
Risk	rs63751160(-;-)
Alt	rs63751160(-;-)
Reference	Rs63751160(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639666delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076702.2,