rs1060502032

Orientation

plus

Stabilized

plus

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

Make rs1060502032(G;T)

Make rs1060502032(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47476522

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1060502032
dbSNP (classic)	rs1060502032
ClinGen	rs1060502032
ebi	rs1060502032
HLI	rs1060502032
Exac	rs1060502032
Gnomad	rs1060502032
Varsome	rs1060502032
LitVar	rs1060502032
Map	rs1060502032
PheGenI	rs1060502032
Biobank	rs1060502032
1000 genomes	rs1060502032
hgdp	rs1060502032
ensembl	rs1060502032
geneview	rs1060502032
scholar	rs1060502032
google	rs1060502032
pharmgkb	rs1060502032
gwascentral	rs1060502032
openSNP	rs1060502032
23andMe	rs1060502032
SNPshot	rs1060502032
SNPdbe	rs1060502032
MSV3d	rs1060502032
GWAS Ctlg	rs1060502032

Max Magnitude

0

ClinVar
Risk	rs1060502032(T;T)
Alt	rs1060502032(T;T)
Reference	Rs1060502032(G;G)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47703661G>T
CLNSRC
CLNACC	RCV000460606.1,