rs63750786

Orientation

plus

Stabilized

plus

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

Make rs63750786(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410319

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750786
dbSNP (classic)	rs63750786
ClinGen	rs63750786
ebi	rs63750786
HLI	rs63750786
Exac	rs63750786
Gnomad	rs63750786
Varsome	rs63750786
LitVar	rs63750786
Map	rs63750786
PheGenI	rs63750786
Biobank	rs63750786
1000 genomes	rs63750786
hgdp	rs63750786
ensembl	rs63750786
geneview	rs63750786
scholar	rs63750786
google	rs63750786
pharmgkb	rs63750786
gwascentral	rs63750786
openSNP	rs63750786
23andMe	rs63750786
SNPshot	rs63750786
SNPdbe	rs63750786
MSV3d	rs63750786
GWAS Ctlg	rs63750786

Max Magnitude

6

ClinVar
Risk	rs63750786(G;G)
Alt	rs63750786(G;G)
Reference	Rs63750786(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637458dupG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076648.2,