rs587782281

Orientation

plus

Stabilized

plus

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

Make rs587782281(-;-)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47796013

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587782281
dbSNP (classic)	rs587782281
ClinGen	rs587782281
ebi	rs587782281
HLI	rs587782281
Exac	rs587782281
Gnomad	rs587782281
Varsome	rs587782281
LitVar	rs587782281
Map	rs587782281
PheGenI	rs587782281
Biobank	rs587782281
1000 genomes	rs587782281
hgdp	rs587782281
ensembl	rs587782281
geneview	rs587782281
scholar	rs587782281
google	rs587782281
pharmgkb	rs587782281
gwascentral	rs587782281
openSNP	rs587782281
23andMe	rs587782281
SNPshot	rs587782281
SNPdbe	rs587782281
MSV3d	rs587782281
GWAS Ctlg	rs587782281

Merged from

Rs786201043

Max Magnitude

6

ClinVar
Risk	rs587782281(-;-)
Alt	rs587782281(-;-)
Reference	Rs587782281(T;T)
Significance	Pathogenic
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.48023153delT
CLNSRC
CLNACC	RCV000162426.3, RCV000231303.1, RCV000480253.1,