rs1064795960

Orientation

plus

Stabilized

plus

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

Chromosome

2

Position

47800105

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1064795960
dbSNP (classic)	rs1064795960
ClinGen	rs1064795960
ebi	rs1064795960
HLI	rs1064795960
Exac	rs1064795960
Gnomad	rs1064795960
Varsome	rs1064795960
LitVar	rs1064795960
Map	rs1064795960
PheGenI	rs1064795960
Biobank	rs1064795960
1000 genomes	rs1064795960
hgdp	rs1064795960
ensembl	rs1064795960
geneview	rs1064795960
scholar	rs1064795960
google	rs1064795960
pharmgkb	rs1064795960
gwascentral	rs1064795960
openSNP	rs1064795960
23andMe	rs1064795960
SNPshot	rs1064795960
SNPdbe	rs1064795960
MSV3d	rs1064795960
GWAS Ctlg	rs1064795960

Max Magnitude

0

ClinVar
Risk	rs1064795960(T;T)
Alt	rs1064795960(T;T)
Reference	Rs1064795960(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.48027244G>T
CLNSRC
CLNACC	RCV000486081.1, RCV000491313.1,