rs63750806

Orientation

plus

Stabilized

plus

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

Make rs63750806(GT;GT)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47475124

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750806
dbSNP (classic)	rs63750806
ClinGen	rs63750806
ebi	rs63750806
HLI	rs63750806
Exac	rs63750806
Gnomad	rs63750806
Varsome	rs63750806
LitVar	rs63750806
Map	rs63750806
PheGenI	rs63750806
Biobank	rs63750806
1000 genomes	rs63750806
hgdp	rs63750806
ensembl	rs63750806
geneview	rs63750806
scholar	rs63750806
google	rs63750806
pharmgkb	rs63750806
gwascentral	rs63750806
openSNP	rs63750806
23andMe	rs63750806
SNPshot	rs63750806
SNPdbe	rs63750806
MSV3d	rs63750806
GWAS Ctlg	rs63750806

Max Magnitude

6

ClinVar
Risk	rs63750806(GT;GT) rs63750806(TG;TG)
Alt	rs63750806(GT;GT) rs63750806(TG;TG)
Reference	Rs63750806(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47702262_47702263dupGT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076304.2,