rs1060502023

Orientation

plus

Stabilized

plus

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

Make rs1060502023(C;C)

Make rs1060502023(C;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47463156

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1060502023
dbSNP (classic)	rs1060502023
ClinGen	rs1060502023
ebi	rs1060502023
HLI	rs1060502023
Exac	rs1060502023
Gnomad	rs1060502023
Varsome	rs1060502023
LitVar	rs1060502023
Map	rs1060502023
PheGenI	rs1060502023
Biobank	rs1060502023
1000 genomes	rs1060502023
hgdp	rs1060502023
ensembl	rs1060502023
geneview	rs1060502023
scholar	rs1060502023
google	rs1060502023
pharmgkb	rs1060502023
gwascentral	rs1060502023
openSNP	rs1060502023
23andMe	rs1060502023
SNPshot	rs1060502023
SNPdbe	rs1060502023
MSV3d	rs1060502023
GWAS Ctlg	rs1060502023

Max Magnitude

0

ClinVar
Risk	rs1060502023(C;C)
Alt	rs1060502023(C;C)
Reference	Rs1060502023(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.47690295T>C
CLNSRC
CLNACC	RCV000461276.1, RCV000491134.1,