rs63751326

Orientation

plus

Stabilized

plus

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

Make rs63751326(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410304

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751326
dbSNP (classic)	rs63751326
ClinGen	rs63751326
ebi	rs63751326
HLI	rs63751326
Exac	rs63751326
Gnomad	rs63751326
Varsome	rs63751326
LitVar	rs63751326
Map	rs63751326
PheGenI	rs63751326
Biobank	rs63751326
1000 genomes	rs63751326
hgdp	rs63751326
ensembl	rs63751326
geneview	rs63751326
scholar	rs63751326
google	rs63751326
pharmgkb	rs63751326
gwascentral	rs63751326
openSNP	rs63751326
23andMe	rs63751326
SNPshot	rs63751326
SNPdbe	rs63751326
MSV3d	rs63751326
GWAS Ctlg	rs63751326

Max Magnitude

6

ClinVar
Risk	rs63751326(T;T)
Alt	rs63751326(T;T)
Reference	Rs63751326(C;C)
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.47637443C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076645.2, RCV000490948.1,