rs63751226

Orientation

plus

Stabilized

plus

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

Make rs63751226(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47410199

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751226
dbSNP (classic)	rs63751226
ClinGen	rs63751226
ebi	rs63751226
HLI	rs63751226
Exac	rs63751226
Gnomad	rs63751226
Varsome	rs63751226
LitVar	rs63751226
Map	rs63751226
PheGenI	rs63751226
Biobank	rs63751226
1000 genomes	rs63751226
hgdp	rs63751226
ensembl	rs63751226
geneview	rs63751226
scholar	rs63751226
google	rs63751226
pharmgkb	rs63751226
gwascentral	rs63751226
openSNP	rs63751226
23andMe	rs63751226
SNPshot	rs63751226
SNPdbe	rs63751226
MSV3d	rs63751226
GWAS Ctlg	rs63751226

Max Magnitude

6

ClinVar
Risk	rs63751226(T;T)
Alt	rs63751226(T;T)
Reference	Rs63751226(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637338C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076605.2,