rs63749915

Orientation

plus

Stabilized

plus

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

Make rs63749915(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47414377

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749915
dbSNP (classic)	rs63749915
ClinGen	rs63749915
ebi	rs63749915
HLI	rs63749915
Exac	rs63749915
Gnomad	rs63749915
Varsome	rs63749915
LitVar	rs63749915
Map	rs63749915
PheGenI	rs63749915
Biobank	rs63749915
1000 genomes	rs63749915
hgdp	rs63749915
ensembl	rs63749915
geneview	rs63749915
scholar	rs63749915
google	rs63749915
pharmgkb	rs63749915
gwascentral	rs63749915
openSNP	rs63749915
23andMe	rs63749915
SNPshot	rs63749915
SNPdbe	rs63749915
MSV3d	rs63749915
GWAS Ctlg	rs63749915

Max Magnitude

6

ClinVar
Risk	rs63749915(T;T)
Alt	rs63749915(T;T)
Reference	Rs63749915(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47641516A>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076746.2,