rs63750885

Orientation

plus

Stabilized

plus

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

Make rs63750885(AT;AT)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414375

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750885
dbSNP (classic)	rs63750885
ClinGen	rs63750885
ebi	rs63750885
HLI	rs63750885
Exac	rs63750885
Gnomad	rs63750885
Varsome	rs63750885
LitVar	rs63750885
Map	rs63750885
PheGenI	rs63750885
Biobank	rs63750885
1000 genomes	rs63750885
hgdp	rs63750885
ensembl	rs63750885
geneview	rs63750885
scholar	rs63750885
google	rs63750885
pharmgkb	rs63750885
gwascentral	rs63750885
openSNP	rs63750885
23andMe	rs63750885
SNPshot	rs63750885
SNPdbe	rs63750885
MSV3d	rs63750885
GWAS Ctlg	rs63750885

Max Magnitude

6

ClinVar
Risk	rs63750885(TA;TA)
Alt	rs63750885(TA;TA)
Reference	Rs63750885(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641513_47641514dup; NC_000002.11:g.47641513_47641514dupAT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000491733.1, RCV000076745.2,