rs767319284

Orientation

plus

Stabilized

plus

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

Make rs767319284(G;G)

Reference

GRCh38.p7 38.3/149

Chromosome

11

Position

64804620

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs767319284
dbSNP (classic)	rs767319284
ClinGen	rs767319284
ebi	rs767319284
HLI	rs767319284
Exac	rs767319284
Gnomad	rs767319284
Varsome	rs767319284
LitVar	rs767319284
Map	rs767319284
PheGenI	rs767319284
Biobank	rs767319284
1000 genomes	rs767319284
hgdp	rs767319284
ensembl	rs767319284
geneview	rs767319284
scholar	rs767319284
google	rs767319284
pharmgkb	rs767319284
gwascentral	rs767319284
openSNP	rs767319284
23andMe	rs767319284
SNPshot	rs767319284
SNPdbe	rs767319284
MSV3d	rs767319284
GWAS Ctlg	rs767319284

Max Magnitude

5.8

ClinVar
Risk	rs767319284(G;G)
Alt	rs767319284(G;G)
Reference	Rs767319284(-;-)
Significance	Pathogenic
Disease	not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	not provided Hereditary cancer-predisposing syndrome
Reversed	0
HGVS	NC_000011.9:g.64572093dupG
CLNSRC
CLNACC	RCV000269197.1, RCV000491230.1,