rs587779232

Orientation

plus

Stabilized

plus

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

Make rs587779232(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800110

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779232
dbSNP (classic)	rs587779232
ClinGen	rs587779232
ebi	rs587779232
HLI	rs587779232
Exac	rs587779232
Gnomad	rs587779232
Varsome	rs587779232
LitVar	rs587779232
Map	rs587779232
PheGenI	rs587779232
Biobank	rs587779232
1000 genomes	rs587779232
hgdp	rs587779232
ensembl	rs587779232
geneview	rs587779232
scholar	rs587779232
google	rs587779232
pharmgkb	rs587779232
gwascentral	rs587779232
openSNP	rs587779232
23andMe	rs587779232
SNPshot	rs587779232
SNPdbe	rs587779232
MSV3d	rs587779232
GWAS Ctlg	rs587779232

Max Magnitude

6

ClinVar
Risk	rs587779232(A;A)
Alt	rs587779232(A;A)
Reference	Rs587779232(T;T)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48027249T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074719.2, RCV000130308.4,