rs63751142

Orientation

plus

Stabilized

plus

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

Make rs63751142(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47429887

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751142
dbSNP (classic)	rs63751142
ClinGen	rs63751142
ebi	rs63751142
HLI	rs63751142
Exac	rs63751142
Gnomad	rs63751142
Varsome	rs63751142
LitVar	rs63751142
Map	rs63751142
PheGenI	rs63751142
Biobank	rs63751142
1000 genomes	rs63751142
hgdp	rs63751142
ensembl	rs63751142
geneview	rs63751142
scholar	rs63751142
google	rs63751142
pharmgkb	rs63751142
gwascentral	rs63751142
openSNP	rs63751142
23andMe	rs63751142
SNPshot	rs63751142
SNPdbe	rs63751142
MSV3d	rs63751142
GWAS Ctlg	rs63751142

Max Magnitude

6

ClinVar
Risk	rs63751142(T;T)
Alt	rs63751142(T;T)
Reference	Rs63751142(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47657026dup; NC_000002.11:g.47657026dupT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000491975.1, RCV000076069.2, RCV000479156.1,