rs63749878

Orientation

plus

Stabilized

plus

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

Make rs63749878(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47476432

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749878
dbSNP (classic)	rs63749878
ClinGen	rs63749878
ebi	rs63749878
HLI	rs63749878
Exac	rs63749878
Gnomad	rs63749878
Varsome	rs63749878
LitVar	rs63749878
Map	rs63749878
PheGenI	rs63749878
Biobank	rs63749878
1000 genomes	rs63749878
hgdp	rs63749878
ensembl	rs63749878
geneview	rs63749878
scholar	rs63749878
google	rs63749878
pharmgkb	rs63749878
gwascentral	rs63749878
openSNP	rs63749878
23andMe	rs63749878
SNPshot	rs63749878
SNPdbe	rs63749878
MSV3d	rs63749878
GWAS Ctlg	rs63749878

Max Magnitude

6

ClinVar
Risk	rs63749878(A;A)
Alt	rs63749878(A;A)
Reference	Rs63749878(-;-)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703571dupA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076379.2,