rs1060502891

Orientation

plus

Stabilized

plus

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

Make rs1060502891(-;-)

Make rs1060502891(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47803500

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502891
dbSNP (classic)	rs1060502891
ClinGen	rs1060502891
ebi	rs1060502891
HLI	rs1060502891
Exac	rs1060502891
Gnomad	rs1060502891
Varsome	rs1060502891
LitVar	rs1060502891
Map	rs1060502891
PheGenI	rs1060502891
Biobank	rs1060502891
1000 genomes	rs1060502891
hgdp	rs1060502891
ensembl	rs1060502891
geneview	rs1060502891
scholar	rs1060502891
google	rs1060502891
pharmgkb	rs1060502891
gwascentral	rs1060502891
openSNP	rs1060502891
23andMe	rs1060502891
SNPshot	rs1060502891
SNPdbe	rs1060502891
MSV3d	rs1060502891
GWAS Ctlg	rs1060502891

Max Magnitude

0

ClinVar
Risk	rs1060502891(-;-)
Alt	rs1060502891(-;-)
Reference	Rs1060502891(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48030639delA
CLNSRC
CLNACC	RCV000460971.1,