rs63751044

Orientation

plus

Stabilized

plus

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

Make rs63751044(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47416323

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751044
dbSNP (classic)	rs63751044
ClinGen	rs63751044
ebi	rs63751044
HLI	rs63751044
Exac	rs63751044
Gnomad	rs63751044
Varsome	rs63751044
LitVar	rs63751044
Map	rs63751044
PheGenI	rs63751044
Biobank	rs63751044
1000 genomes	rs63751044
hgdp	rs63751044
ensembl	rs63751044
geneview	rs63751044
scholar	rs63751044
google	rs63751044
pharmgkb	rs63751044
gwascentral	rs63751044
openSNP	rs63751044
23andMe	rs63751044
SNPshot	rs63751044
SNPdbe	rs63751044
MSV3d	rs63751044
GWAS Ctlg	rs63751044

Max Magnitude

6

ClinVar
Risk	rs63751044(-;-)
Alt	rs63751044(-;-)
Reference	Rs63751044(CA;CA)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47643462_47643463delCA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076767.2,