rs786201043

Merged into

rs587782281

Orientation

plus

Stabilized

plus

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

Make rs786201043(-;-)

Make rs786201043(-;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47796014

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs786201043
dbSNP (classic)	rs786201043
ClinGen	rs786201043
ebi	rs786201043
HLI	rs786201043
Exac	rs786201043
Gnomad	rs786201043
Varsome	rs786201043
LitVar	rs786201043
Map	rs786201043
PheGenI	rs786201043
Biobank	rs786201043
1000 genomes	rs786201043
hgdp	rs786201043
ensembl	rs786201043
geneview	rs786201043
scholar	rs786201043
google	rs786201043
pharmgkb	rs786201043
gwascentral	rs786201043
openSNP	rs786201043
23andMe	rs786201043
SNPshot	rs786201043
SNPdbe	rs786201043
MSV3d	rs786201043
GWAS Ctlg	rs786201043

Status

Merged into rs587782281

Max Magnitude

0

ClinVar
Risk
Alt
Reference	Rs786201043(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Lynch syndrome
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome Lynch syndrome
Reversed	0
HGVS	NC_000002.11:g.48023153delT
CLNSRC
CLNACC	RCV000162426.2, RCV000231303.1,