rs786202108

Orientation

plus

Stabilized

plus

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

Make rs786202108(-;-)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47799755

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs786202108
dbSNP (classic)	rs786202108
ClinGen	rs786202108
ebi	rs786202108
HLI	rs786202108
Exac	rs786202108
Gnomad	rs786202108
Varsome	rs786202108
LitVar	rs786202108
Map	rs786202108
PheGenI	rs786202108
Biobank	rs786202108
1000 genomes	rs786202108
hgdp	rs786202108
ensembl	rs786202108
geneview	rs786202108
scholar	rs786202108
google	rs786202108
pharmgkb	rs786202108
gwascentral	rs786202108
openSNP	rs786202108
23andMe	rs786202108
SNPshot	rs786202108
SNPdbe	rs786202108
MSV3d	rs786202108
GWAS Ctlg	rs786202108

Merged from

Rs768876235

Max Magnitude

6

ClinVar
Risk	rs786202108(-;-)
Alt	rs786202108(-;-)
Reference	Rs786202108(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026894delC
CLNSRC
CLNACC	RCV000164756.2,