rs863224526

Orientation

minus

Stabilized

minus

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

Make rs863224526(G;T)

Make rs863224526(T;T)

Reference

GRCh38.p2 38.2/146

Chromosome

11

Position

64804738

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs863224526
dbSNP (classic)	rs863224526
ClinGen	rs863224526
ebi	rs863224526
HLI	rs863224526
Exac	rs863224526
Gnomad	rs863224526
Varsome	rs863224526
LitVar	rs863224526
Map	rs863224526
PheGenI	rs863224526
Biobank	rs863224526
1000 genomes	rs863224526
hgdp	rs863224526
ensembl	rs863224526
geneview	rs863224526
scholar	rs863224526
google	rs863224526
pharmgkb	rs863224526
gwascentral	rs863224526
openSNP	rs863224526
23andMe	rs863224526
SNPshot	rs863224526
SNPdbe	rs863224526
MSV3d	rs863224526
GWAS Ctlg	rs863224526

Max Magnitude

0

ClinVar
Risk	rs863224526(T;T)
Alt	rs863224526(T;T)
Reference	Rs863224526(G;G)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	Multiple endocrine neoplasia, type 1 not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64572210C>A
CLNSRC
CLNACC	RCV000198067.2, RCV000254822.2, RCV000490934.1,