rs63750069

Orientation

plus

Stabilized

plus

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

Make rs63750069(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410245

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750069
dbSNP (classic)	rs63750069
ClinGen	rs63750069
ebi	rs63750069
HLI	rs63750069
Exac	rs63750069
Gnomad	rs63750069
Varsome	rs63750069
LitVar	rs63750069
Map	rs63750069
PheGenI	rs63750069
Biobank	rs63750069
1000 genomes	rs63750069
hgdp	rs63750069
ensembl	rs63750069
geneview	rs63750069
scholar	rs63750069
google	rs63750069
pharmgkb	rs63750069
gwascentral	rs63750069
openSNP	rs63750069
23andMe	rs63750069
SNPshot	rs63750069
SNPdbe	rs63750069
MSV3d	rs63750069
GWAS Ctlg	rs63750069

Max Magnitude

6

ClinVar
Risk	rs63750069(-;-)
Alt	rs63750069(-;-)
Reference	Rs63750069(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637384delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076627.2,