rs104894261

Orientation

minus

Stabilized

minus

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

Make rs104894261(T;T)

Reference

GRCh38 38.1/141

Chromosome

11

Position

64804588

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs104894261
dbSNP (classic)	rs104894261
ClinGen	rs104894261
ebi	rs104894261
HLI	rs104894261
Exac	rs104894261
Gnomad	rs104894261
Varsome	rs104894261
LitVar	rs104894261
Map	rs104894261
PheGenI	rs104894261
Biobank	rs104894261
1000 genomes	rs104894261
hgdp	rs104894261
ensembl	rs104894261
geneview	rs104894261
scholar	rs104894261
google	rs104894261
pharmgkb	rs104894261
gwascentral	rs104894261
openSNP	rs104894261
23andMe	rs104894261
SNPshot	rs104894261
SNPdbe	rs104894261
MSV3d	rs104894261
GWAS Ctlg	rs104894261

Max Magnitude

5.8

OMIM	131100
Desc
Variant	0012
Related	also

ClinVar
Risk	rs104894261(T;T)
Alt	rs104894261(T;T)
Reference	Rs104894261(C;C)
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.64572060G>A
CLNSRC	OMIM Allelic Variant
CLNACC	RCV000018168.2, RCV000182423.3, RCV000491431.1,