rs1060502001

Orientation

plus

Stabilized

plus

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

Make rs1060502001(A;T)

Make rs1060502001(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47403276

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1060502001
dbSNP (classic)	rs1060502001
ClinGen	rs1060502001
ebi	rs1060502001
HLI	rs1060502001
Exac	rs1060502001
Gnomad	rs1060502001
Varsome	rs1060502001
LitVar	rs1060502001
Map	rs1060502001
PheGenI	rs1060502001
Biobank	rs1060502001
1000 genomes	rs1060502001
hgdp	rs1060502001
ensembl	rs1060502001
geneview	rs1060502001
scholar	rs1060502001
google	rs1060502001
pharmgkb	rs1060502001
gwascentral	rs1060502001
openSNP	rs1060502001
23andMe	rs1060502001
SNPshot	rs1060502001
SNPdbe	rs1060502001
MSV3d	rs1060502001
GWAS Ctlg	rs1060502001

Max Magnitude

0

ClinVar
Risk	rs1060502001(T;T)
Alt	rs1060502001(T;T)
Reference	Rs1060502001(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47630415A>T
CLNSRC
CLNACC	RCV000467909.1,