rs786203712

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;-)	0	common in clinvar
(-;C)	6	Lynch syndrome
(D;D)	0	common genotype

Make rs786203712(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47803514

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs786203712
dbSNP (classic)	rs786203712
ClinGen	rs786203712
ebi	rs786203712
HLI	rs786203712
Exac	rs786203712
Gnomad	rs786203712
Varsome	rs786203712
LitVar	rs786203712
Map	rs786203712
PheGenI	rs786203712
Biobank	rs786203712
1000 genomes	rs786203712
hgdp	rs786203712
ensembl	rs786203712
geneview	rs786203712
scholar	rs786203712
google	rs786203712
pharmgkb	rs786203712
gwascentral	rs786203712
openSNP	rs786203712
23andMe	rs786203712
SNPshot	rs786203712
SNPdbe	rs786203712
MSV3d	rs786203712
GWAS Ctlg	rs786203712

Max Magnitude

6

ClinVar
Risk	Rs786203712(A;A) rs786203712(C;C)
Alt	Rs786203712(A;A) rs786203712(C;C)
Reference	Rs786203712(-;-)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48030653_48030654insC; NC_000002.11:g.48030653dupA
CLNSRC
CLNACC	RCV000167133.1, RCV000414406.1,