rs587778533

Orientation

plus

Stabilized

plus

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

Make rs587778533(-;T)

Make rs587778533(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

2

Position

47803554

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs587778533
dbSNP (classic)	rs587778533
ClinGen	rs587778533
ebi	rs587778533
HLI	rs587778533
Exac	rs587778533
Gnomad	rs587778533
Varsome	rs587778533
LitVar	rs587778533
Map	rs587778533
PheGenI	rs587778533
Biobank	rs587778533
1000 genomes	rs587778533
hgdp	rs587778533
ensembl	rs587778533
geneview	rs587778533
scholar	rs587778533
google	rs587778533
pharmgkb	rs587778533
gwascentral	rs587778533
openSNP	rs587778533
23andMe	rs587778533
SNPshot	rs587778533
SNPdbe	rs587778533
MSV3d	rs587778533
GWAS Ctlg	rs587778533

Merged from

Rs587781924

Max Magnitude

0

ClinVar
Risk	rs587778533(T;T)
Alt	rs587778533(T;T)
Reference	Rs587778533(-;-)
Significance	Pathogenic
Disease	not specified Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	not specified Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48030698dupT
CLNSRC
CLNACC	RCV000121582.1, RCV000130275.4,