rs63750426

Orientation

plus

Stabilized

plus

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

Make rs63750426(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47412464

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750426
dbSNP (classic)	rs63750426
ClinGen	rs63750426
ebi	rs63750426
HLI	rs63750426
Exac	rs63750426
Gnomad	rs63750426
Varsome	rs63750426
LitVar	rs63750426
Map	rs63750426
PheGenI	rs63750426
Biobank	rs63750426
1000 genomes	rs63750426
hgdp	rs63750426
ensembl	rs63750426
geneview	rs63750426
scholar	rs63750426
google	rs63750426
pharmgkb	rs63750426
gwascentral	rs63750426
openSNP	rs63750426
23andMe	rs63750426
SNPshot	rs63750426
SNPdbe	rs63750426
MSV3d	rs63750426
GWAS Ctlg	rs63750426

Max Magnitude

6

ClinVar
Risk	rs63750426(-;-)
Alt	rs63750426(-;-)
Reference	Rs63750426(TT;TT)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47639603_47639604delTT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076684.2,