rs63751600

Orientation

plus

Stabilized

plus

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

Make rs63751600(C;C)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47463154

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751600
dbSNP (classic)	rs63751600
ClinGen	rs63751600
ebi	rs63751600
HLI	rs63751600
Exac	rs63751600
Gnomad	rs63751600
Varsome	rs63751600
LitVar	rs63751600
Map	rs63751600
PheGenI	rs63751600
Biobank	rs63751600
1000 genomes	rs63751600
hgdp	rs63751600
ensembl	rs63751600
geneview	rs63751600
scholar	rs63751600
google	rs63751600
pharmgkb	rs63751600
gwascentral	rs63751600
openSNP	rs63751600
23andMe	rs63751600
SNPshot	rs63751600
SNPdbe	rs63751600
MSV3d	rs63751600
GWAS Ctlg	rs63751600

Max Magnitude

6

ClinVar
Risk	rs63751600(C;C) rs63751600(T;T)
Alt	rs63751600(C;C) rs63751600(T;T)
Reference	Rs63751600(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690293G>C
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076181.2,