rs63750346

Orientation

plus

Stabilized

plus

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

Make rs63750346(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478355

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750346
dbSNP (classic)	rs63750346
ClinGen	rs63750346
ebi	rs63750346
HLI	rs63750346
Exac	rs63750346
Gnomad	rs63750346
Varsome	rs63750346
LitVar	rs63750346
Map	rs63750346
PheGenI	rs63750346
Biobank	rs63750346
1000 genomes	rs63750346
hgdp	rs63750346
ensembl	rs63750346
geneview	rs63750346
scholar	rs63750346
google	rs63750346
pharmgkb	rs63750346
gwascentral	rs63750346
openSNP	rs63750346
23andMe	rs63750346
SNPshot	rs63750346
SNPdbe	rs63750346
MSV3d	rs63750346
GWAS Ctlg	rs63750346

Max Magnitude

6

ClinVar
Risk	rs63750346(-;-)
Alt	rs63750346(-;-)
Reference	Rs63750346(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47705494delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076453.2,