rs63751156

Orientation

plus

Stabilized

plus

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

Make rs63751156(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478289

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751156
dbSNP (classic)	rs63751156
ClinGen	rs63751156
ebi	rs63751156
HLI	rs63751156
Exac	rs63751156
Gnomad	rs63751156
Varsome	rs63751156
LitVar	rs63751156
Map	rs63751156
PheGenI	rs63751156
Biobank	rs63751156
1000 genomes	rs63751156
hgdp	rs63751156
ensembl	rs63751156
geneview	rs63751156
scholar	rs63751156
google	rs63751156
pharmgkb	rs63751156
gwascentral	rs63751156
openSNP	rs63751156
23andMe	rs63751156
SNPshot	rs63751156
SNPdbe	rs63751156
MSV3d	rs63751156
GWAS Ctlg	rs63751156

Max Magnitude

6

ClinVar
Risk	rs63751156(-;-)
Alt	rs63751156(-;-)
Reference	Rs63751156(ATTC;ATTC)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47705428_47705431delCATT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076436.2,