rs63750662

Orientation

plus

Stabilized

plus

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

Make rs63750662(GA;GA)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47466786

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750662
dbSNP (classic)	rs63750662
ClinGen	rs63750662
ebi	rs63750662
HLI	rs63750662
Exac	rs63750662
Gnomad	rs63750662
Varsome	rs63750662
LitVar	rs63750662
Map	rs63750662
PheGenI	rs63750662
Biobank	rs63750662
1000 genomes	rs63750662
hgdp	rs63750662
ensembl	rs63750662
geneview	rs63750662
scholar	rs63750662
google	rs63750662
pharmgkb	rs63750662
gwascentral	rs63750662
openSNP	rs63750662
23andMe	rs63750662
SNPshot	rs63750662
SNPdbe	rs63750662
MSV3d	rs63750662
GWAS Ctlg	rs63750662

Max Magnitude

6

ClinVar
Risk	rs63750662(AG;AG)
Alt	rs63750662(AG;AG)
Reference	Rs63750662(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47693924_47693925dupGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076208.2,