rs104894259

Orientation

minus

Stabilized

minus

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

Make rs104894259(C;C)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64805078

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs104894259
dbSNP (classic)	rs104894259
ClinGen	rs104894259
ebi	rs104894259
HLI	rs104894259
Exac	rs104894259
Gnomad	rs104894259
Varsome	rs104894259
LitVar	rs104894259
Map	rs104894259
PheGenI	rs104894259
Biobank	rs104894259
1000 genomes	rs104894259
hgdp	rs104894259
ensembl	rs104894259
geneview	rs104894259
scholar	rs104894259
google	rs104894259
pharmgkb	rs104894259
gwascentral	rs104894259
openSNP	rs104894259
23andMe	rs104894259
SNPshot	rs104894259
SNPdbe	rs104894259
MSV3d	rs104894259
GWAS Ctlg	rs104894259

Max Magnitude

5.8

OMIM	131100
Desc
Variant	0010
Related	also

ClinVar
Risk	rs104894259(A;A) rs104894259(C;C)
Alt	rs104894259(A;A) rs104894259(C;C)
Reference	Rs104894259(T;T)
Significance	Pathogenic
Disease	Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia not provided
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	Hereditary cancer-predisposing syndrome Multiple endocrine neoplasia, type 1 not provided
Reversed	1
HGVS	NC_000011.9:g.64572550A>G; NC_000011.9:g.64572550A>T
CLNSRC	OMIM Allelic Variant UniProtKB (protein)
CLNACC	RCV000491105.1, RCV000018166.3, RCV000255755.1,