rs587782809

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(-;G)	6	Lynch syndrome
(G;G)	0	common in clinvar

Make rs587782809(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47799273

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587782809
dbSNP (classic)	rs587782809
ClinGen	rs587782809
ebi	rs587782809
HLI	rs587782809
Exac	rs587782809
Gnomad	rs587782809
Varsome	rs587782809
LitVar	rs587782809
Map	rs587782809
PheGenI	rs587782809
Biobank	rs587782809
1000 genomes	rs587782809
hgdp	rs587782809
ensembl	rs587782809
geneview	rs587782809
scholar	rs587782809
google	rs587782809
pharmgkb	rs587782809
gwascentral	rs587782809
openSNP	rs587782809
23andMe	rs587782809
SNPshot	rs587782809
SNPdbe	rs587782809
MSV3d	rs587782809
GWAS Ctlg	rs587782809

Max Magnitude

6

ClinVar
Risk	rs587782809(-;-)
Alt	rs587782809(-;-)
Reference	Rs587782809(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48026412delG
CLNSRC
CLNACC	RCV000132371.2,