rs63750384

Orientation

plus

Stabilized

plus

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

Make rs63750384(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47463052

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750384
dbSNP (classic)	rs63750384
ClinGen	rs63750384
ebi	rs63750384
HLI	rs63750384
Exac	rs63750384
Gnomad	rs63750384
Varsome	rs63750384
LitVar	rs63750384
Map	rs63750384
PheGenI	rs63750384
Biobank	rs63750384
1000 genomes	rs63750384
hgdp	rs63750384
ensembl	rs63750384
geneview	rs63750384
scholar	rs63750384
google	rs63750384
pharmgkb	rs63750384
gwascentral	rs63750384
openSNP	rs63750384
23andMe	rs63750384
SNPshot	rs63750384
SNPdbe	rs63750384
MSV3d	rs63750384
GWAS Ctlg	rs63750384

Max Magnitude

6

ClinVar
Risk	rs63750384(-;-)
Alt	rs63750384(-;-)
Reference	Rs63750384(G;G)
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.47690191delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076153.2, RCV000491004.1,