rs63751056

Orientation

plus

Stabilized

plus

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

Make rs63751056(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403301

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751056
dbSNP (classic)	rs63751056
ClinGen	rs63751056
ebi	rs63751056
HLI	rs63751056
Exac	rs63751056
Gnomad	rs63751056
Varsome	rs63751056
LitVar	rs63751056
Map	rs63751056
PheGenI	rs63751056
Biobank	rs63751056
1000 genomes	rs63751056
hgdp	rs63751056
ensembl	rs63751056
geneview	rs63751056
scholar	rs63751056
google	rs63751056
pharmgkb	rs63751056
gwascentral	rs63751056
openSNP	rs63751056
23andMe	rs63751056
SNPshot	rs63751056
SNPdbe	rs63751056
MSV3d	rs63751056
GWAS Ctlg	rs63751056

Max Magnitude

6

ClinVar
Risk	rs63751056(-;-)
Alt	rs63751056(-;-)
Reference	Rs63751056(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630440delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076041.2,