rs63751115

Orientation

plus

Stabilized

plus

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

Make rs63751115(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414357

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751115
dbSNP (classic)	rs63751115
ClinGen	rs63751115
ebi	rs63751115
HLI	rs63751115
Exac	rs63751115
Gnomad	rs63751115
Varsome	rs63751115
LitVar	rs63751115
Map	rs63751115
PheGenI	rs63751115
Biobank	rs63751115
1000 genomes	rs63751115
hgdp	rs63751115
ensembl	rs63751115
geneview	rs63751115
scholar	rs63751115
google	rs63751115
pharmgkb	rs63751115
gwascentral	rs63751115
openSNP	rs63751115
23andMe	rs63751115
SNPshot	rs63751115
SNPdbe	rs63751115
MSV3d	rs63751115
GWAS Ctlg	rs63751115

Max Magnitude

6

ClinVar
Risk	rs63751115(-;-)
Alt	rs63751115(-;-)
Reference	Rs63751115(TT;TT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641496_47641497delTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076742.2,