rs1064793489

Orientation

plus

Stabilized

plus

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

Chromosome

2

Position

47805028

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1064793489
dbSNP (classic)	rs1064793489
ClinGen	rs1064793489
ebi	rs1064793489
HLI	rs1064793489
Exac	rs1064793489
Gnomad	rs1064793489
Varsome	rs1064793489
LitVar	rs1064793489
Map	rs1064793489
PheGenI	rs1064793489
Biobank	rs1064793489
1000 genomes	rs1064793489
hgdp	rs1064793489
ensembl	rs1064793489
geneview	rs1064793489
scholar	rs1064793489
google	rs1064793489
pharmgkb	rs1064793489
gwascentral	rs1064793489
openSNP	rs1064793489
23andMe	rs1064793489
SNPshot	rs1064793489
SNPdbe	rs1064793489
MSV3d	rs1064793489
GWAS Ctlg	rs1064793489

Max Magnitude

0

ClinVar
Risk	rs1064793489(-;-)
Alt	rs1064793489(-;-)
Reference	Rs1064793489(G;G)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MSH6
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000002.11:g.48032167delG
CLNSRC
CLNACC	RCV000480410.1, RCV000491243.1,