rs121913035

Orientation

minus

Stabilized

minus

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

Make rs121913035(A;T)

Make rs121913035(T;T)

Reference

GRCh38.p2 38.2/144

Chromosome

11

Position

64804513

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs121913035
dbSNP (classic)	rs121913035
ClinGen	rs121913035
ebi	rs121913035
HLI	rs121913035
Exac	rs121913035
Gnomad	rs121913035
Varsome	rs121913035
LitVar	rs121913035
Map	rs121913035
PheGenI	rs121913035
Biobank	rs121913035
1000 genomes	rs121913035
hgdp	rs121913035
ensembl	rs121913035
geneview	rs121913035
scholar	rs121913035
google	rs121913035
pharmgkb	rs121913035
gwascentral	rs121913035
openSNP	rs121913035
23andMe	rs121913035
SNPshot	rs121913035
SNPdbe	rs121913035
MSV3d	rs121913035
GWAS Ctlg	rs121913035

Max Magnitude

0

ClinVar
Risk	rs121913035(T;T)
Alt	rs121913035(T;T)
Reference	Rs121913035(A;A)
Significance	Pathogenic
Disease	Adenoma of the adrenal gland
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	Adenoma of the adrenal gland
Reversed	1
HGVS	NC_000011.9:g.64571985T>A
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000018178.4,