rs794728634

Orientation

minus

Stabilized

minus

Geno	Mag	Summary
(C;T)	5.8	Multiple Endocrine Neoplasia Type 1
(T;T)	0	common in clinvar

Make rs794728634(C;C)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64804437

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs794728634
dbSNP (classic)	rs794728634
ClinGen	rs794728634
ebi	rs794728634
HLI	rs794728634
Exac	rs794728634
Gnomad	rs794728634
Varsome	rs794728634
LitVar	rs794728634
Map	rs794728634
PheGenI	rs794728634
Biobank	rs794728634
1000 genomes	rs794728634
hgdp	rs794728634
ensembl	rs794728634
geneview	rs794728634
scholar	rs794728634
google	rs794728634
pharmgkb	rs794728634
gwascentral	rs794728634
openSNP	rs794728634
23andMe	rs794728634
SNPshot	rs794728634
SNPdbe	rs794728634
MSV3d	rs794728634
GWAS Ctlg	rs794728634

Max Magnitude

5.8

ClinVar
Risk	rs794728634(C;C)
Alt	rs794728634(C;C)
Reference	Rs794728634(T;T)
Significance	Probable-Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64571909A>G
CLNSRC
CLNACC	RCV000182428.3, RCV000491331.1,