rs1060501991

Orientation

plus

Stabilized

plus

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

Make rs1060501991(A;A)

Make rs1060501991(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47480695

Gene

MSH2

is a	snp
is	mentioned by
dbSNP	rs1060501991
dbSNP (classic)	rs1060501991
ClinGen	rs1060501991
ebi	rs1060501991
HLI	rs1060501991
Exac	rs1060501991
Gnomad	rs1060501991
Varsome	rs1060501991
LitVar	rs1060501991
Map	rs1060501991
PheGenI	rs1060501991
Biobank	rs1060501991
1000 genomes	rs1060501991
hgdp	rs1060501991
ensembl	rs1060501991
geneview	rs1060501991
scholar	rs1060501991
google	rs1060501991
pharmgkb	rs1060501991
gwascentral	rs1060501991
openSNP	rs1060501991
23andMe	rs1060501991
SNPshot	rs1060501991
SNPdbe	rs1060501991
MSV3d	rs1060501991
GWAS Ctlg	rs1060501991

Max Magnitude

0

ClinVar
Risk	rs1060501991(A;A)
Alt	rs1060501991(A;A)
Reference	Rs1060501991(G;G)
Significance	Probable-Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH2
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.47707834G>A
CLNSRC
CLNACC	RCV000465186.1,