rs63750545

Orientation

plus

Stabilized

plus

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

Make rs63750545(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476502

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750545
dbSNP (classic)	rs63750545
ClinGen	rs63750545
ebi	rs63750545
HLI	rs63750545
Exac	rs63750545
Gnomad	rs63750545
Varsome	rs63750545
LitVar	rs63750545
Map	rs63750545
PheGenI	rs63750545
Biobank	rs63750545
1000 genomes	rs63750545
hgdp	rs63750545
ensembl	rs63750545
geneview	rs63750545
scholar	rs63750545
google	rs63750545
pharmgkb	rs63750545
gwascentral	rs63750545
openSNP	rs63750545
23andMe	rs63750545
SNPshot	rs63750545
SNPdbe	rs63750545
MSV3d	rs63750545
GWAS Ctlg	rs63750545

Max Magnitude

6

ClinVar
Risk	rs63750545(C;C)
Alt	rs63750545(C;C)
Reference	Rs63750545(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703641dupC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076410.2,