rs104894264

Orientation

minus

Stabilized

minus

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

Make rs104894264(A;A)

Make rs104894264(A;G)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64805132

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs104894264
dbSNP (classic)	rs104894264
ClinGen	rs104894264
ebi	rs104894264
HLI	rs104894264
Exac	rs104894264
Gnomad	rs104894264
Varsome	rs104894264
LitVar	rs104894264
Map	rs104894264
PheGenI	rs104894264
Biobank	rs104894264
1000 genomes	rs104894264
hgdp	rs104894264
ensembl	rs104894264
geneview	rs104894264
scholar	rs104894264
google	rs104894264
pharmgkb	rs104894264
gwascentral	rs104894264
openSNP	rs104894264
23andMe	rs104894264
SNPshot	rs104894264
SNPdbe	rs104894264
MSV3d	rs104894264
GWAS Ctlg	rs104894264

Max Magnitude

0

OMIM	131100
Desc
Variant	0027
Related	also

ClinVar
Risk	rs104894264(A;A) rs104894264(C;C) rs104894264(T;T)
Alt	rs104894264(A;A) rs104894264(C;C) rs104894264(T;T)
Reference	Rs104894264(G;G)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome not provided Multiple endocrine neoplasia
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	Hereditary cancer-predisposing syndrome not provided Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64572604C>A; NC_000011.9:g.64572604C>G; NC_000011.9:g.64572604C>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000491697.1, RCV000182455.2, RCV000018183.5, RCV000490854.1,