rs587779267

Orientation

plus

Stabilized

plus

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

Make rs587779267(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47804958

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779267
dbSNP (classic)	rs587779267
ClinGen	rs587779267
ebi	rs587779267
HLI	rs587779267
Exac	rs587779267
Gnomad	rs587779267
Varsome	rs587779267
LitVar	rs587779267
Map	rs587779267
PheGenI	rs587779267
Biobank	rs587779267
1000 genomes	rs587779267
hgdp	rs587779267
ensembl	rs587779267
geneview	rs587779267
scholar	rs587779267
google	rs587779267
pharmgkb	rs587779267
gwascentral	rs587779267
openSNP	rs587779267
23andMe	rs587779267
SNPshot	rs587779267
SNPdbe	rs587779267
MSV3d	rs587779267
GWAS Ctlg	rs587779267

Max Magnitude

6

aka c.3487G>T, p.Glu1163Ter, E1163X and E1163*

ClinVar
Risk	rs587779267(T;T)
Alt	rs587779267(T;T)
Reference	Rs587779267(G;G)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48032097G>T
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074867.2, RCV000115417.2, RCV000491292.1,