rs1060502886

Orientation

plus

Stabilized

plus

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

Make rs1060502886(-;-)

Make rs1060502886(-;TA)

Reference

GRCh38.p7 38.3/150

Chromosome

2

Position

47799798

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1060502886
dbSNP (classic)	rs1060502886
ClinGen	rs1060502886
ebi	rs1060502886
HLI	rs1060502886
Exac	rs1060502886
Gnomad	rs1060502886
Varsome	rs1060502886
LitVar	rs1060502886
Map	rs1060502886
PheGenI	rs1060502886
Biobank	rs1060502886
1000 genomes	rs1060502886
hgdp	rs1060502886
ensembl	rs1060502886
geneview	rs1060502886
scholar	rs1060502886
google	rs1060502886
pharmgkb	rs1060502886
gwascentral	rs1060502886
openSNP	rs1060502886
23andMe	rs1060502886
SNPshot	rs1060502886
SNPdbe	rs1060502886
MSV3d	rs1060502886
GWAS Ctlg	rs1060502886

Max Magnitude

0

ClinVar
Risk	rs1060502886(-;-)
Alt	rs1060502886(-;-)
Reference	Rs1060502886(TA;TA)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026937_48026938delTA
CLNSRC
CLNACC	RCV000470844.1, RCV000486089.1, RCV000491721.1,