rs63750881

Orientation

plus

Stabilized

plus

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

Make rs63750881(A;C)

Make rs63750881(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47412504

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750881
dbSNP (classic)	rs63750881
ClinGen	rs63750881
ebi	rs63750881
HLI	rs63750881
Exac	rs63750881
Gnomad	rs63750881
Varsome	rs63750881
LitVar	rs63750881
Map	rs63750881
PheGenI	rs63750881
Biobank	rs63750881
1000 genomes	rs63750881
hgdp	rs63750881
ensembl	rs63750881
geneview	rs63750881
scholar	rs63750881
google	rs63750881
pharmgkb	rs63750881
gwascentral	rs63750881
openSNP	rs63750881
23andMe	rs63750881
SNPshot	rs63750881
SNPdbe	rs63750881
MSV3d	rs63750881
GWAS Ctlg	rs63750881

Max Magnitude

6

ClinVar
Risk	rs63750881(C;C) rs63750881(T;T)
Alt	rs63750881(C;C) rs63750881(T;T)
Reference	Rs63750881(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639643A>C; NC_000002.11:g.47639643A>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000076695.2, RCV000076696.2,