rs786203968

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(A;A)	0	common in clinvar
(A;T)	6	Lynch syndrome

Make rs786203968(A;C)

Make rs786203968(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47804997

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs786203968
dbSNP (classic)	rs786203968
ClinGen	rs786203968
ebi	rs786203968
HLI	rs786203968
Exac	rs786203968
Gnomad	rs786203968
Varsome	rs786203968
LitVar	rs786203968
Map	rs786203968
PheGenI	rs786203968
Biobank	rs786203968
1000 genomes	rs786203968
hgdp	rs786203968
ensembl	rs786203968
geneview	rs786203968
scholar	rs786203968
google	rs786203968
pharmgkb	rs786203968
gwascentral	rs786203968
openSNP	rs786203968
23andMe	rs786203968
SNPshot	rs786203968
SNPdbe	rs786203968
MSV3d	rs786203968
GWAS Ctlg	rs786203968

Max Magnitude

6

ClinVar
Risk	rs786203968(C;C) rs786203968(T;T)
Alt	rs786203968(C;C) rs786203968(T;T)
Reference	Rs786203968(A;A)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48032136A>C; NC_000002.11:g.48032136A>T
CLNSRC
CLNACC	RCV000167501.1, RCV000204275.1,