rs63749975

Orientation

plus

Stabilized

plus

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

Make rs63749975(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47480766

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749975
dbSNP (classic)	rs63749975
ClinGen	rs63749975
ebi	rs63749975
HLI	rs63749975
Exac	rs63749975
Gnomad	rs63749975
Varsome	rs63749975
LitVar	rs63749975
Map	rs63749975
PheGenI	rs63749975
Biobank	rs63749975
1000 genomes	rs63749975
hgdp	rs63749975
ensembl	rs63749975
geneview	rs63749975
scholar	rs63749975
google	rs63749975
pharmgkb	rs63749975
gwascentral	rs63749975
openSNP	rs63749975
23andMe	rs63749975
SNPshot	rs63749975
SNPdbe	rs63749975
MSV3d	rs63749975
GWAS Ctlg	rs63749975

Max Magnitude

6

ClinVar
Risk	rs63749975(-;-)
Alt	rs63749975(-;-)
Reference	Rs63749975(GT;GT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707905_47707906delTG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076496.2,