rs587779208

Orientation

plus

Stabilized

plus

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

Make rs587779208(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47799176

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779208
dbSNP (classic)	rs587779208
ClinGen	rs587779208
ebi	rs587779208
HLI	rs587779208
Exac	rs587779208
Gnomad	rs587779208
Varsome	rs587779208
LitVar	rs587779208
Map	rs587779208
PheGenI	rs587779208
Biobank	rs587779208
1000 genomes	rs587779208
hgdp	rs587779208
ensembl	rs587779208
geneview	rs587779208
scholar	rs587779208
google	rs587779208
pharmgkb	rs587779208
gwascentral	rs587779208
openSNP	rs587779208
23andMe	rs587779208
SNPshot	rs587779208
SNPdbe	rs587779208
MSV3d	rs587779208
GWAS Ctlg	rs587779208

Max Magnitude

6

ClinVar
Risk	rs587779208(A;A)
Alt	rs587779208(A;A)
Reference	Rs587779208(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48026315T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074641.2,