rs63750701

Orientation

plus

Stabilized

plus

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

Make rs63750701(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414330

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750701
dbSNP (classic)	rs63750701
ClinGen	rs63750701
ebi	rs63750701
HLI	rs63750701
Exac	rs63750701
Gnomad	rs63750701
Varsome	rs63750701
LitVar	rs63750701
Map	rs63750701
PheGenI	rs63750701
Biobank	rs63750701
1000 genomes	rs63750701
hgdp	rs63750701
ensembl	rs63750701
geneview	rs63750701
scholar	rs63750701
google	rs63750701
pharmgkb	rs63750701
gwascentral	rs63750701
openSNP	rs63750701
23andMe	rs63750701
SNPshot	rs63750701
SNPdbe	rs63750701
MSV3d	rs63750701
GWAS Ctlg	rs63750701

Max Magnitude

6

ClinVar
Risk	rs63750701(-;-)
Alt	rs63750701(-;-)
Reference	Rs63750701(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641469delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076736.2,