rs63751429

Orientation

plus

Stabilized

plus

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

Make rs63751429(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47408466

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751429
dbSNP (classic)	rs63751429
ClinGen	rs63751429
ebi	rs63751429
HLI	rs63751429
Exac	rs63751429
Gnomad	rs63751429
Varsome	rs63751429
LitVar	rs63751429
Map	rs63751429
PheGenI	rs63751429
Biobank	rs63751429
1000 genomes	rs63751429
hgdp	rs63751429
ensembl	rs63751429
geneview	rs63751429
scholar	rs63751429
google	rs63751429
pharmgkb	rs63751429
gwascentral	rs63751429
openSNP	rs63751429
23andMe	rs63751429
SNPshot	rs63751429
SNPdbe	rs63751429
MSV3d	rs63751429
GWAS Ctlg	rs63751429

Max Magnitude

6

ClinVar
Risk	rs63751429(T;T)
Alt	rs63751429(T;T)
Reference	Rs63751429(C;C)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47635605C>T
CLNSRC	UniProtKB (protein)
CLNACC	RCV000076546.2,