rs1064793169

Orientation

minus

Stabilized

minus

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

Chromosome

11

Position

64806359

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1064793169
dbSNP (classic)	rs1064793169
ClinGen	rs1064793169
ebi	rs1064793169
HLI	rs1064793169
Exac	rs1064793169
Gnomad	rs1064793169
Varsome	rs1064793169
LitVar	rs1064793169
Map	rs1064793169
PheGenI	rs1064793169
Biobank	rs1064793169
1000 genomes	rs1064793169
hgdp	rs1064793169
ensembl	rs1064793169
geneview	rs1064793169
scholar	rs1064793169
google	rs1064793169
pharmgkb	rs1064793169
gwascentral	rs1064793169
openSNP	rs1064793169
23andMe	rs1064793169
SNPshot	rs1064793169
SNPdbe	rs1064793169
MSV3d	rs1064793169
GWAS Ctlg	rs1064793169

Max Magnitude

0

ClinVar
Risk	rs1064793169(C;C)
Alt	rs1064793169(C;C)
Reference	Rs1064793169(T;T)
Significance	Probable-Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64573831A>G
CLNSRC
CLNACC	RCV000482667.1, RCV000491064.1,