rs63750234

Orientation

plus

Stabilized

plus

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

Make rs63750234(A;A)

Make rs63750234(A;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476381

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750234
dbSNP (classic)	rs63750234
ClinGen	rs63750234
ebi	rs63750234
HLI	rs63750234
Exac	rs63750234
Gnomad	rs63750234
Varsome	rs63750234
LitVar	rs63750234
Map	rs63750234
PheGenI	rs63750234
Biobank	rs63750234
1000 genomes	rs63750234
hgdp	rs63750234
ensembl	rs63750234
geneview	rs63750234
scholar	rs63750234
google	rs63750234
pharmgkb	rs63750234
gwascentral	rs63750234
openSNP	rs63750234
23andMe	rs63750234
SNPshot	rs63750234
SNPdbe	rs63750234
MSV3d	rs63750234
GWAS Ctlg	rs63750234

Max Magnitude

6

ClinVar
Risk	rs63750234(A;A) rs63750234(C;C)
Alt	rs63750234(A;A) rs63750234(C;C)
Reference	Rs63750234(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703520G>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000076362.2,