rs63750334

Orientation

plus

Stabilized

plus

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

Make rs63750334(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403336

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750334
dbSNP (classic)	rs63750334
ClinGen	rs63750334
ebi	rs63750334
HLI	rs63750334
Exac	rs63750334
Gnomad	rs63750334
Varsome	rs63750334
LitVar	rs63750334
Map	rs63750334
PheGenI	rs63750334
Biobank	rs63750334
1000 genomes	rs63750334
hgdp	rs63750334
ensembl	rs63750334
geneview	rs63750334
scholar	rs63750334
google	rs63750334
pharmgkb	rs63750334
gwascentral	rs63750334
openSNP	rs63750334
23andMe	rs63750334
SNPshot	rs63750334
SNPdbe	rs63750334
MSV3d	rs63750334
GWAS Ctlg	rs63750334

Max Magnitude

6

ClinVar
Risk	rs63750334(-;-)
Alt	rs63750334(-;-)
Reference	Rs63750334(GA;GA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630475_47630476delGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076168.2,