rs587781544

Orientation

plus

Stabilized

plus

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

Make rs587781544(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47803663

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587781544
dbSNP (classic)	rs587781544
ClinGen	rs587781544
ebi	rs587781544
HLI	rs587781544
Exac	rs587781544
Gnomad	rs587781544
Varsome	rs587781544
LitVar	rs587781544
Map	rs587781544
PheGenI	rs587781544
Biobank	rs587781544
1000 genomes	rs587781544
hgdp	rs587781544
ensembl	rs587781544
geneview	rs587781544
scholar	rs587781544
google	rs587781544
pharmgkb	rs587781544
gwascentral	rs587781544
openSNP	rs587781544
23andMe	rs587781544
SNPshot	rs587781544
SNPdbe	rs587781544
MSV3d	rs587781544
GWAS Ctlg	rs587781544

Max Magnitude

6

ClinVar
Risk	rs587781544(-;-)
Alt	rs587781544(-;-)
Reference	Rs587781544(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.48030802delG
CLNSRC
CLNACC	RCV000129558.2,