rs63751099

Orientation

plus

Stabilized

plus

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

Make rs63751099(T;T)

Reference

GRCh38 38.1/141

Chromosome

2

Position

47403219

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs63751099
dbSNP (classic)	rs63751099
ClinGen	rs63751099
ebi	rs63751099
HLI	rs63751099
Exac	rs63751099
Gnomad	rs63751099
Varsome	rs63751099
LitVar	rs63751099
Map	rs63751099
PheGenI	rs63751099
Biobank	rs63751099
1000 genomes	rs63751099
hgdp	rs63751099
ensembl	rs63751099
geneview	rs63751099
scholar	rs63751099
google	rs63751099
pharmgkb	rs63751099
gwascentral	rs63751099
openSNP	rs63751099
23andMe	rs63751099
SNPshot	rs63751099
SNPdbe	rs63751099
MSV3d	rs63751099
GWAS Ctlg	rs63751099

Max Magnitude

6

ClinVar
Risk	rs63751099(A;A) rs63751099(T;T)
Alt	rs63751099(A;A) rs63751099(T;T)
Reference	Rs63751099(C;C)
Significance	Pathogenic
Disease	not provided Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	not provided Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630358C>A; NC_000002.11:g.47630358C>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000034557.1, RCV000076557.2,