rs63750161

Orientation

plus

Stabilized

plus

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

Make rs63750161(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47463091

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750161
dbSNP (classic)	rs63750161
ClinGen	rs63750161
ebi	rs63750161
HLI	rs63750161
Exac	rs63750161
Gnomad	rs63750161
Varsome	rs63750161
LitVar	rs63750161
Map	rs63750161
PheGenI	rs63750161
Biobank	rs63750161
1000 genomes	rs63750161
hgdp	rs63750161
ensembl	rs63750161
geneview	rs63750161
scholar	rs63750161
google	rs63750161
pharmgkb	rs63750161
gwascentral	rs63750161
openSNP	rs63750161
23andMe	rs63750161
SNPshot	rs63750161
SNPdbe	rs63750161
MSV3d	rs63750161
GWAS Ctlg	rs63750161

Max Magnitude

6

ClinVar
Risk	rs63750161(-;-)
Alt	rs63750161(-;-)
Reference	Rs63750161(AG;AG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690230_47690231delGA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076165.2,