rs63749850

Orientation

plus

Stabilized

plus

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

Make rs63749850(CA;CA)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429862

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749850
dbSNP (classic)	rs63749850
ClinGen	rs63749850
ebi	rs63749850
HLI	rs63749850
Exac	rs63749850
Gnomad	rs63749850
Varsome	rs63749850
LitVar	rs63749850
Map	rs63749850
PheGenI	rs63749850
Biobank	rs63749850
1000 genomes	rs63749850
hgdp	rs63749850
ensembl	rs63749850
geneview	rs63749850
scholar	rs63749850
google	rs63749850
pharmgkb	rs63749850
gwascentral	rs63749850
openSNP	rs63749850
23andMe	rs63749850
SNPshot	rs63749850
SNPdbe	rs63749850
MSV3d	rs63749850
GWAS Ctlg	rs63749850

Max Magnitude

6

ClinVar
Risk	rs63749850(CA;CA)
Alt	rs63749850(CA;CA)
Reference	Rs63749850(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47657000_47657001dupCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076058.2,