rs876660943

Orientation

plus

Stabilized

plus

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

Make rs876660943(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47806359

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876660943
dbSNP (classic)	rs876660943
ClinGen	rs876660943
ebi	rs876660943
HLI	rs876660943
Exac	rs876660943
Gnomad	rs876660943
Varsome	rs876660943
LitVar	rs876660943
Map	rs876660943
PheGenI	rs876660943
Biobank	rs876660943
1000 genomes	rs876660943
hgdp	rs876660943
ensembl	rs876660943
geneview	rs876660943
scholar	rs876660943
google	rs876660943
pharmgkb	rs876660943
gwascentral	rs876660943
openSNP	rs876660943
23andMe	rs876660943
SNPshot	rs876660943
SNPdbe	rs876660943
MSV3d	rs876660943
GWAS Ctlg	rs876660943

Max Magnitude

6

ClinVar
Risk	rs876660943(T;T)
Alt	rs876660943(T;T)
Reference	Rs876660943(G;G)
Significance	Probable-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.48033498G>T
CLNSRC
CLNACC	RCV000217114.1, RCV000226322.1,