rs63750986

Orientation

plus

Stabilized

plus

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

Make rs63750986(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47463101

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750986
dbSNP (classic)	rs63750986
ClinGen	rs63750986
ebi	rs63750986
HLI	rs63750986
Exac	rs63750986
Gnomad	rs63750986
Varsome	rs63750986
LitVar	rs63750986
Map	rs63750986
PheGenI	rs63750986
Biobank	rs63750986
1000 genomes	rs63750986
hgdp	rs63750986
ensembl	rs63750986
geneview	rs63750986
scholar	rs63750986
google	rs63750986
pharmgkb	rs63750986
gwascentral	rs63750986
openSNP	rs63750986
23andMe	rs63750986
SNPshot	rs63750986
SNPdbe	rs63750986
MSV3d	rs63750986
GWAS Ctlg	rs63750986

Max Magnitude

6

ClinVar
Risk	rs63750986(-;-)
Alt	rs63750986(-;-)
Reference	Rs63750986(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690240delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076167.2,