rs63750984

Orientation

plus

Stabilized

plus

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

Make rs63750984(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403310

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750984
dbSNP (classic)	rs63750984
ClinGen	rs63750984
ebi	rs63750984
HLI	rs63750984
Exac	rs63750984
Gnomad	rs63750984
Varsome	rs63750984
LitVar	rs63750984
Map	rs63750984
PheGenI	rs63750984
Biobank	rs63750984
1000 genomes	rs63750984
hgdp	rs63750984
ensembl	rs63750984
geneview	rs63750984
scholar	rs63750984
google	rs63750984
pharmgkb	rs63750984
gwascentral	rs63750984
openSNP	rs63750984
23andMe	rs63750984
SNPshot	rs63750984
SNPdbe	rs63750984
MSV3d	rs63750984
GWAS Ctlg	rs63750984

Max Magnitude

6

ClinVar
Risk	rs63750984(-;-)
Alt	rs63750984(-;-)
Reference	Rs63750984(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630449delG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076059.2,