rs587782275

Merged into

rs267608058

Orientation

plus

Stabilized

plus

Geno	Mag	Summary
(CAGT;CAGT)	0	common in clinvar

Make rs587782275(-;-)

Make rs587782275(-;CAGT)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47800130

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587782275
dbSNP (classic)	rs587782275
ClinGen	rs587782275
ebi	rs587782275
HLI	rs587782275
Exac	rs587782275
Gnomad	rs587782275
Varsome	rs587782275
LitVar	rs587782275
Map	rs587782275
PheGenI	rs587782275
Biobank	rs587782275
1000 genomes	rs587782275
hgdp	rs587782275
ensembl	rs587782275
geneview	rs587782275
scholar	rs587782275
google	rs587782275
pharmgkb	rs587782275
gwascentral	rs587782275
openSNP	rs587782275
23andMe	rs587782275
SNPshot	rs587782275
SNPdbe	rs587782275
MSV3d	rs587782275
GWAS Ctlg	rs587782275

Status

Merged into rs267608058

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs587782275(CAGT;CAGT)
Significance	Pathogenic
Disease	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48027272_48027275delTCAG
CLNSRC	International Society for Gastrointestinal Hereditary Tumours
CLNACC	RCV000074720.2, RCV000162408.2, RCV000202111.2,