rs63750828

Orientation

plus

Stabilized

plus

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

Make rs63750828(A;A)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47416351

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750828
dbSNP (classic)	rs63750828
ClinGen	rs63750828
ebi	rs63750828
HLI	rs63750828
Exac	rs63750828
Gnomad	rs63750828
Varsome	rs63750828
LitVar	rs63750828
Map	rs63750828
PheGenI	rs63750828
Biobank	rs63750828
1000 genomes	rs63750828
hgdp	rs63750828
ensembl	rs63750828
geneview	rs63750828
scholar	rs63750828
google	rs63750828
pharmgkb	rs63750828
gwascentral	rs63750828
openSNP	rs63750828
23andMe	rs63750828
SNPshot	rs63750828
SNPdbe	rs63750828
MSV3d	rs63750828
GWAS Ctlg	rs63750828

Max Magnitude

6

ClinVar
Risk	rs63750828(A;A)
Alt	rs63750828(A;A)
Reference	Rs63750828(G;G)
Significance	Pathogenic
Disease	Lynch syndrome I not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome I not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47643490G>A
CLNSRC	UniProtKB (protein)
CLNACC	RCV000076778.2, RCV000160579.5, RCV000216069.2,