rs587779245

Orientation

plus

Stabilized

plus

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

Make rs587779245(A;A)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800697

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779245
dbSNP (classic)	rs587779245
ClinGen	rs587779245
ebi	rs587779245
HLI	rs587779245
Exac	rs587779245
Gnomad	rs587779245
Varsome	rs587779245
LitVar	rs587779245
Map	rs587779245
PheGenI	rs587779245
Biobank	rs587779245
1000 genomes	rs587779245
hgdp	rs587779245
ensembl	rs587779245
geneview	rs587779245
scholar	rs587779245
google	rs587779245
pharmgkb	rs587779245
gwascentral	rs587779245
openSNP	rs587779245
23andMe	rs587779245
SNPshot	rs587779245
SNPdbe	rs587779245
MSV3d	rs587779245
GWAS Ctlg	rs587779245

Max Magnitude

6

c.2714T>A (p.Leu905Ter)

23andMe name: i5046132

ClinVar
Risk	rs587779245(A;A)
Alt	rs587779245(A;A)
Reference	Rs587779245(T;T)
Significance	Pathogenic
Disease	Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48027836T>A
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074775.2,