rs1060502882

Orientation

plus

Stabilized

plus

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

Make rs1060502882(-;-)

Make rs1060502882(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47801132

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502882
dbSNP (classic)	rs1060502882
ClinGen	rs1060502882
ebi	rs1060502882
HLI	rs1060502882
Exac	rs1060502882
Gnomad	rs1060502882
Varsome	rs1060502882
LitVar	rs1060502882
Map	rs1060502882
PheGenI	rs1060502882
Biobank	rs1060502882
1000 genomes	rs1060502882
hgdp	rs1060502882
ensembl	rs1060502882
geneview	rs1060502882
scholar	rs1060502882
google	rs1060502882
pharmgkb	rs1060502882
gwascentral	rs1060502882
openSNP	rs1060502882
23andMe	rs1060502882
SNPshot	rs1060502882
SNPdbe	rs1060502882
MSV3d	rs1060502882
GWAS Ctlg	rs1060502882

Max Magnitude

0

ClinVar
Risk	rs1060502882(-;-)
Alt	rs1060502882(-;-)
Reference	Rs1060502882(C;C)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48028271delC
CLNSRC
CLNACC	RCV000473512.1,