rs63750961

Orientation

plus

Stabilized

plus

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

Make rs63750961(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476450

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750961
dbSNP (classic)	rs63750961
ClinGen	rs63750961
ebi	rs63750961
HLI	rs63750961
Exac	rs63750961
Gnomad	rs63750961
Varsome	rs63750961
LitVar	rs63750961
Map	rs63750961
PheGenI	rs63750961
Biobank	rs63750961
1000 genomes	rs63750961
hgdp	rs63750961
ensembl	rs63750961
geneview	rs63750961
scholar	rs63750961
google	rs63750961
pharmgkb	rs63750961
gwascentral	rs63750961
openSNP	rs63750961
23andMe	rs63750961
SNPshot	rs63750961
SNPdbe	rs63750961
MSV3d	rs63750961
GWAS Ctlg	rs63750961

Max Magnitude

6

ClinVar
Risk	rs63750961(C;C)
Alt	rs63750961(C;C)
Reference	Rs63750961(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703589T>C
CLNSRC	UniProtKB (protein)
CLNACC	RCV000076384.2,