rs1060502890

Orientation

plus

Stabilized

plus

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

Make rs1060502890(-;-)

Make rs1060502890(-;A)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47800974

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502890
dbSNP (classic)	rs1060502890
ClinGen	rs1060502890
ebi	rs1060502890
HLI	rs1060502890
Exac	rs1060502890
Gnomad	rs1060502890
Varsome	rs1060502890
LitVar	rs1060502890
Map	rs1060502890
PheGenI	rs1060502890
Biobank	rs1060502890
1000 genomes	rs1060502890
hgdp	rs1060502890
ensembl	rs1060502890
geneview	rs1060502890
scholar	rs1060502890
google	rs1060502890
pharmgkb	rs1060502890
gwascentral	rs1060502890
openSNP	rs1060502890
23andMe	rs1060502890
SNPshot	rs1060502890
SNPdbe	rs1060502890
MSV3d	rs1060502890
GWAS Ctlg	rs1060502890

Max Magnitude

0

ClinVar
Risk	rs1060502890(-;-)
Alt	rs1060502890(-;-)
Reference	Rs1060502890(A;A)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48028113delA
CLNSRC
CLNACC	RCV000472587.1,