rs63750508

Orientation

plus

Stabilized

plus

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

Make rs63750508(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47475126

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750508
dbSNP (classic)	rs63750508
ClinGen	rs63750508
ebi	rs63750508
HLI	rs63750508
Exac	rs63750508
Gnomad	rs63750508
Varsome	rs63750508
LitVar	rs63750508
Map	rs63750508
PheGenI	rs63750508
Biobank	rs63750508
1000 genomes	rs63750508
hgdp	rs63750508
ensembl	rs63750508
geneview	rs63750508
scholar	rs63750508
google	rs63750508
pharmgkb	rs63750508
gwascentral	rs63750508
openSNP	rs63750508
23andMe	rs63750508
SNPshot	rs63750508
SNPdbe	rs63750508
MSV3d	rs63750508
GWAS Ctlg	rs63750508

Max Magnitude

6

ClinVar
Risk	rs63750508(G;G) rs63750508(T;T)
Alt	rs63750508(G;G) rs63750508(T;T)
Reference	Rs63750508(C;C)
Significance	Pathogenic
Disease	Lynch syndrome not specified not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome not specified not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47702265C>G; NC_000002.11:g.47702265C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000465743.1, RCV000483159.1, RCV000076305.2, RCV000414448.1, RCV000491286.1,