rs1064795629

Orientation

plus

Stabilized

plus

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

Chromosome

2

Position

47806204

Gene

MSH6

is a	snp
is	mentioned by
dbSNP	rs1064795629
dbSNP (classic)	rs1064795629
ClinGen	rs1064795629
ebi	rs1064795629
HLI	rs1064795629
Exac	rs1064795629
Gnomad	rs1064795629
Varsome	rs1064795629
LitVar	rs1064795629
Map	rs1064795629
PheGenI	rs1064795629
Biobank	rs1064795629
1000 genomes	rs1064795629
hgdp	rs1064795629
ensembl	rs1064795629
geneview	rs1064795629
scholar	rs1064795629
google	rs1064795629
pharmgkb	rs1064795629
gwascentral	rs1064795629
openSNP	rs1064795629
23andMe	rs1064795629
SNPshot	rs1064795629
SNPdbe	rs1064795629
MSV3d	rs1064795629
GWAS Ctlg	rs1064795629

Max Magnitude

0

ClinVar
Risk	rs1064795629(-;-)
Alt	rs1064795629(-;-)
Reference	Rs1064795629(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.48033343delG
CLNSRC
CLNACC	RCV000481123.1, RCV000491618.1,