rs63751315

Orientation

plus

Stabilized

plus

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

Make rs63751315(A;A)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47445563

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751315
dbSNP (classic)	rs63751315
ClinGen	rs63751315
ebi	rs63751315
HLI	rs63751315
Exac	rs63751315
Gnomad	rs63751315
Varsome	rs63751315
LitVar	rs63751315
Map	rs63751315
PheGenI	rs63751315
Biobank	rs63751315
1000 genomes	rs63751315
hgdp	rs63751315
ensembl	rs63751315
geneview	rs63751315
scholar	rs63751315
google	rs63751315
pharmgkb	rs63751315
gwascentral	rs63751315
openSNP	rs63751315
23andMe	rs63751315
SNPshot	rs63751315
SNPdbe	rs63751315
MSV3d	rs63751315
GWAS Ctlg	rs63751315

Max Magnitude

6

ClinVar
Risk	rs63751315(A;A)
Alt	rs63751315(A;A)
Reference	Rs63751315(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47672702T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000076116.2,