rs1060502029

Orientation

plus

Stabilized

plus

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

Make rs1060502029(AAA;AAA)

Make rs1060502029(AAA;GAAG)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47463114

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1060502029
dbSNP (classic)	rs1060502029
ClinGen	rs1060502029
ebi	rs1060502029
HLI	rs1060502029
Exac	rs1060502029
Gnomad	rs1060502029
Varsome	rs1060502029
LitVar	rs1060502029
Map	rs1060502029
PheGenI	rs1060502029
Biobank	rs1060502029
1000 genomes	rs1060502029
hgdp	rs1060502029
ensembl	rs1060502029
geneview	rs1060502029
scholar	rs1060502029
google	rs1060502029
pharmgkb	rs1060502029
gwascentral	rs1060502029
openSNP	rs1060502029
23andMe	rs1060502029
SNPshot	rs1060502029
SNPdbe	rs1060502029
MSV3d	rs1060502029
GWAS Ctlg	rs1060502029

Max Magnitude

0

ClinVar
Risk	rs1060502029(AAA;AAA)
Alt	rs1060502029(AAA;AAA)
Reference	Rs1060502029(GAAG;GAAG)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47690253_47690256delGAAGinsAAA
CLNSRC
CLNACC	RCV000470495.1,