rs63751621

Orientation

plus

Stabilized

plus

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

Make rs63751621(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47480703

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751621
dbSNP (classic)	rs63751621
ClinGen	rs63751621
ebi	rs63751621
HLI	rs63751621
Exac	rs63751621
Gnomad	rs63751621
Varsome	rs63751621
LitVar	rs63751621
Map	rs63751621
PheGenI	rs63751621
Biobank	rs63751621
1000 genomes	rs63751621
hgdp	rs63751621
ensembl	rs63751621
geneview	rs63751621
scholar	rs63751621
google	rs63751621
pharmgkb	rs63751621
gwascentral	rs63751621
openSNP	rs63751621
23andMe	rs63751621
SNPshot	rs63751621
SNPdbe	rs63751621
MSV3d	rs63751621
GWAS Ctlg	rs63751621

Max Magnitude

6

ClinVar
Risk	rs63751621(-;-)
Alt	rs63751621(-;-)
Reference	Rs63751621(TG;TG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707842_47707843delTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076483.2,