rs63750463

Orientation

plus

Stabilized

plus

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

Make rs63750463(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478423

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750463
dbSNP (classic)	rs63750463
ClinGen	rs63750463
ebi	rs63750463
HLI	rs63750463
Exac	rs63750463
Gnomad	rs63750463
Varsome	rs63750463
LitVar	rs63750463
Map	rs63750463
PheGenI	rs63750463
Biobank	rs63750463
1000 genomes	rs63750463
hgdp	rs63750463
ensembl	rs63750463
geneview	rs63750463
scholar	rs63750463
google	rs63750463
pharmgkb	rs63750463
gwascentral	rs63750463
openSNP	rs63750463
23andMe	rs63750463
SNPshot	rs63750463
SNPdbe	rs63750463
MSV3d	rs63750463
GWAS Ctlg	rs63750463

Max Magnitude

6

ClinVar
Risk	rs63750463(A;A)
Alt	rs63750463(A;A)
Reference	Rs63750463(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation	info
Gene	MSH2
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.47705562dup; NC_000002.11:g.47705562dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000490851.1, RCV000076464.2, RCV000480512.1,