rs876660095

Orientation

plus

Stabilized

plus

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

Make rs876660095(T;T)

Reference

GRCh38.p2 38.2/147

Chromosome

2

Position

47783236

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs876660095
dbSNP (classic)	rs876660095
ClinGen	rs876660095
ebi	rs876660095
HLI	rs876660095
Exac	rs876660095
Gnomad	rs876660095
Varsome	rs876660095
LitVar	rs876660095
Map	rs876660095
PheGenI	rs876660095
Biobank	rs876660095
1000 genomes	rs876660095
hgdp	rs876660095
ensembl	rs876660095
geneview	rs876660095
scholar	rs876660095
google	rs876660095
pharmgkb	rs876660095
gwascentral	rs876660095
openSNP	rs876660095
23andMe	rs876660095
SNPshot	rs876660095
SNPdbe	rs876660095
MSV3d	rs876660095
GWAS Ctlg	rs876660095

Max Magnitude

6

ClinVar
Risk	rs876660095(T;T)
Alt	rs876660095(T;T)
Reference	Rs876660095(G;G)
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.48010375G>T
CLNSRC
CLNACC	RCV000219646.2, RCV000485238.1,