rs587782712

Orientation

plus

Stabilized

plus

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

Make rs587782712(-;-)

Make rs587782712(AAGAA;AAGAA)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47801020

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587782712
dbSNP (classic)	rs587782712
ClinGen	rs587782712
ebi	rs587782712
HLI	rs587782712
Exac	rs587782712
Gnomad	rs587782712
Varsome	rs587782712
LitVar	rs587782712
Map	rs587782712
PheGenI	rs587782712
Biobank	rs587782712
1000 genomes	rs587782712
hgdp	rs587782712
ensembl	rs587782712
geneview	rs587782712
scholar	rs587782712
google	rs587782712
pharmgkb	rs587782712
gwascentral	rs587782712
openSNP	rs587782712
23andMe	rs587782712
SNPshot	rs587782712
SNPdbe	rs587782712
MSV3d	rs587782712
GWAS Ctlg	rs587782712

Max Magnitude

6

ClinVar
Risk	rs587782712(-;-)
Alt	rs587782712(-;-)
Reference	Rs587782712(GAAAA;GAAAA)
Significance	Other
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48028159_48028163delAAGAA
CLNSRC
CLNACC	RCV000132188.4, RCV000200490.2, RCV000202303.1,