rs63750382

Orientation

plus

Stabilized

plus

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

Make rs63750382(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410256

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63750382
dbSNP (classic)	rs63750382
ClinGen	rs63750382
ebi	rs63750382
HLI	rs63750382
Exac	rs63750382
Gnomad	rs63750382
Varsome	rs63750382
LitVar	rs63750382
Map	rs63750382
PheGenI	rs63750382
Biobank	rs63750382
1000 genomes	rs63750382
hgdp	rs63750382
ensembl	rs63750382
geneview	rs63750382
scholar	rs63750382
google	rs63750382
pharmgkb	rs63750382
gwascentral	rs63750382
openSNP	rs63750382
23andMe	rs63750382
SNPshot	rs63750382
SNPdbe	rs63750382
MSV3d	rs63750382
GWAS Ctlg	rs63750382

Max Magnitude

6

ClinVar
Risk	rs63750382(A;A) rs63750382(T;T)
Alt	rs63750382(A;A) rs63750382(T;T)
Reference	Rs63750382(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637395G>A; NC_000002.11:g.47637395G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076631.2, RCV000076632.2,