rs1064795256

Orientation

plus

Stabilized

plus

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

Chromosome

2

Position

47799697

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1064795256
dbSNP (classic)	rs1064795256
ClinGen	rs1064795256
ebi	rs1064795256
HLI	rs1064795256
Exac	rs1064795256
Gnomad	rs1064795256
Varsome	rs1064795256
LitVar	rs1064795256
Map	rs1064795256
PheGenI	rs1064795256
Biobank	rs1064795256
1000 genomes	rs1064795256
hgdp	rs1064795256
ensembl	rs1064795256
geneview	rs1064795256
scholar	rs1064795256
google	rs1064795256
pharmgkb	rs1064795256
gwascentral	rs1064795256
openSNP	rs1064795256
23andMe	rs1064795256
SNPshot	rs1064795256
SNPdbe	rs1064795256
MSV3d	rs1064795256
GWAS Ctlg	rs1064795256

Max Magnitude

0

ClinVar
Risk	rs1064795256(G;G) rs1064795256(T;T)
Alt	rs1064795256(G;G) rs1064795256(T;T)
Reference	Rs1064795256(C;C)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided
Variation	info
Gene	MSH6
CLNDBN	Hereditary cancer-predisposing syndrome not provided
Reversed	0
HGVS	NC_000002.11:g.48026836C>G; NC_000002.11:g.48026836C>T
CLNSRC
CLNACC	RCV000491403.1, RCV000487144.1,