rs587782425

Orientation

plus

Stabilized

plus

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

Make rs587782425(-;C)

Make rs587782425(C;C)

Reference

GRCh38.p2 38.2/144

Chromosome

2

Position

47803501

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587782425
dbSNP (classic)	rs587782425
ClinGen	rs587782425
ebi	rs587782425
HLI	rs587782425
Exac	rs587782425
Gnomad	rs587782425
Varsome	rs587782425
LitVar	rs587782425
Map	rs587782425
PheGenI	rs587782425
Biobank	rs587782425
1000 genomes	rs587782425
hgdp	rs587782425
ensembl	rs587782425
geneview	rs587782425
scholar	rs587782425
google	rs587782425
pharmgkb	rs587782425
gwascentral	rs587782425
openSNP	rs587782425
23andMe	rs587782425
SNPshot	rs587782425
SNPdbe	rs587782425
MSV3d	rs587782425
GWAS Ctlg	rs587782425

Max Magnitude

0

ClinVar
Risk	rs587782425(C;C)
Alt	rs587782425(C;C)
Reference	Rs587782425(-;-)
Significance	Pathogenic
Disease	Lynch syndrome not provided Hereditary cancer-predisposing syndrome Hereditary nonpolyposis colorectal cancer type 5
Variation	info
Gene	MSH6
CLNDBN	Lynch syndrome not provided Hereditary cancer-predisposing syndrome Hereditary nonpolyposis colorectal cancer type 5
Reversed	0
HGVS	NC_000002.11:g.48030647dupC
CLNSRC	HGMD
CLNACC	RCV000074831.3, RCV000078312.6, RCV000115412.6, RCV000410401.1,