rs63750738

Orientation

plus

Stabilized

plus

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

Make rs63750738(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47466725

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750738
dbSNP (classic)	rs63750738
ClinGen	rs63750738
ebi	rs63750738
HLI	rs63750738
Exac	rs63750738
Gnomad	rs63750738
Varsome	rs63750738
LitVar	rs63750738
Map	rs63750738
PheGenI	rs63750738
Biobank	rs63750738
1000 genomes	rs63750738
hgdp	rs63750738
ensembl	rs63750738
geneview	rs63750738
scholar	rs63750738
google	rs63750738
pharmgkb	rs63750738
gwascentral	rs63750738
openSNP	rs63750738
23andMe	rs63750738
SNPshot	rs63750738
SNPdbe	rs63750738
MSV3d	rs63750738
GWAS Ctlg	rs63750738

Max Magnitude

6

ClinVar
Risk	rs63750738(-;-)
Alt	rs63750738(-;-)
Reference	Rs63750738(C;C)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47693864delC
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076200.2, RCV000492027.1,