rs63749993

Orientation

plus

Stabilized

plus

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

Make rs63749993(G;G)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476424

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749993
dbSNP (classic)	rs63749993
ClinGen	rs63749993
ebi	rs63749993
HLI	rs63749993
Exac	rs63749993
Gnomad	rs63749993
Varsome	rs63749993
LitVar	rs63749993
Map	rs63749993
PheGenI	rs63749993
Biobank	rs63749993
1000 genomes	rs63749993
hgdp	rs63749993
ensembl	rs63749993
geneview	rs63749993
scholar	rs63749993
google	rs63749993
pharmgkb	rs63749993
gwascentral	rs63749993
openSNP	rs63749993
23andMe	rs63749993
SNPshot	rs63749993
SNPdbe	rs63749993
MSV3d	rs63749993
GWAS Ctlg	rs63749993

Max Magnitude

6

ClinVar
Risk	rs63749993(G;G)
Alt	rs63749993(G;G)
Reference	Rs63749993(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47703563T>G
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076376.2, RCV000491088.1,