rs1060502027

Orientation

plus

Stabilized

plus

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

Make rs1060502027(-;-)

Make rs1060502027(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47463049

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1060502027
dbSNP (classic)	rs1060502027
ClinGen	rs1060502027
ebi	rs1060502027
HLI	rs1060502027
Exac	rs1060502027
Gnomad	rs1060502027
Varsome	rs1060502027
LitVar	rs1060502027
Map	rs1060502027
PheGenI	rs1060502027
Biobank	rs1060502027
1000 genomes	rs1060502027
hgdp	rs1060502027
ensembl	rs1060502027
geneview	rs1060502027
scholar	rs1060502027
google	rs1060502027
pharmgkb	rs1060502027
gwascentral	rs1060502027
openSNP	rs1060502027
23andMe	rs1060502027
SNPshot	rs1060502027
SNPdbe	rs1060502027
MSV3d	rs1060502027
GWAS Ctlg	rs1060502027

Max Magnitude

0

ClinVar
Risk	rs1060502027(-;-)
Alt	rs1060502027(-;-)
Reference	Rs1060502027(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690188delC
CLNSRC
CLNACC	RCV000470990.1,