rs587779216

Orientation

plus

Stabilized

plus

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

Make rs587779216(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47799573

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587779216
dbSNP (classic)	rs587779216
ClinGen	rs587779216
ebi	rs587779216
HLI	rs587779216
Exac	rs587779216
Gnomad	rs587779216
Varsome	rs587779216
LitVar	rs587779216
Map	rs587779216
PheGenI	rs587779216
Biobank	rs587779216
1000 genomes	rs587779216
hgdp	rs587779216
ensembl	rs587779216
geneview	rs587779216
scholar	rs587779216
google	rs587779216
pharmgkb	rs587779216
gwascentral	rs587779216
openSNP	rs587779216
23andMe	rs587779216
SNPshot	rs587779216
SNPdbe	rs587779216
MSV3d	rs587779216
GWAS Ctlg	rs587779216

Max Magnitude

6

ClinVar
Risk	rs587779216(-;-)
Alt	rs587779216(-;-)
Reference	Rs587779216(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.48026712delT
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074667.2, RCV000491242.1,