rs63749832

Orientation

plus

Stabilized

plus

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

Make rs63749832(-;-)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47412514

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63749832
dbSNP (classic)	rs63749832
ClinGen	rs63749832
ebi	rs63749832
HLI	rs63749832
Exac	rs63749832
Gnomad	rs63749832
Varsome	rs63749832
LitVar	rs63749832
Map	rs63749832
PheGenI	rs63749832
Biobank	rs63749832
1000 genomes	rs63749832
hgdp	rs63749832
ensembl	rs63749832
geneview	rs63749832
scholar	rs63749832
google	rs63749832
pharmgkb	rs63749832
gwascentral	rs63749832
openSNP	rs63749832
23andMe	rs63749832
SNPshot	rs63749832
SNPdbe	rs63749832
MSV3d	rs63749832
GWAS Ctlg	rs63749832

Max Magnitude

6

ClinVar
Risk	rs63749832(-;-)
Alt	rs63749832(-;-)
Reference	Rs63749832(A;A)
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.47639653delA
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076699.2, RCV000164791.1,