rs63751105

Orientation

plus

Stabilized

plus

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

Make rs63751105(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47478353

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751105
dbSNP (classic)	rs63751105
ClinGen	rs63751105
ebi	rs63751105
HLI	rs63751105
Exac	rs63751105
Gnomad	rs63751105
Varsome	rs63751105
LitVar	rs63751105
Map	rs63751105
PheGenI	rs63751105
Biobank	rs63751105
1000 genomes	rs63751105
hgdp	rs63751105
ensembl	rs63751105
geneview	rs63751105
scholar	rs63751105
google	rs63751105
pharmgkb	rs63751105
gwascentral	rs63751105
openSNP	rs63751105
23andMe	rs63751105
SNPshot	rs63751105
SNPdbe	rs63751105
MSV3d	rs63751105
GWAS Ctlg	rs63751105

Max Magnitude

6

ClinVar
Risk	rs63751105(A;A) rs63751105(C;C)
Alt	rs63751105(A;A) rs63751105(C;C)
Reference	Rs63751105(G;G)
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.47705492G>A; NC_000002.11:g.47705492G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076451.2, RCV000076452.2, RCV000491833.1,