rs1060501989

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(C;C)	0	common in clinvar

Make rs1060501989(C;T)

Make rs1060501989(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47410115

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1060501989
dbSNP (classic)	rs1060501989
ClinGen	rs1060501989
ebi	rs1060501989
HLI	rs1060501989
Exac	rs1060501989
Gnomad	rs1060501989
Varsome	rs1060501989
LitVar	rs1060501989
Map	rs1060501989
PheGenI	rs1060501989
Biobank	rs1060501989
1000 genomes	rs1060501989
hgdp	rs1060501989
ensembl	rs1060501989
geneview	rs1060501989
scholar	rs1060501989
google	rs1060501989
pharmgkb	rs1060501989
gwascentral	rs1060501989
openSNP	rs1060501989
23andMe	rs1060501989
SNPshot	rs1060501989
SNPdbe	rs1060501989
MSV3d	rs1060501989
GWAS Ctlg	rs1060501989

Max Magnitude

0

ClinVar
Risk	rs1060501989(T;T)
Alt	rs1060501989(T;T)
Reference	Rs1060501989(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47637254C>T
CLNSRC
CLNACC	RCV000471483.1,