rs1060499991

Orientation

minus

Stabilized

minus

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

Make rs1060499991(A;A)

Make rs1060499991(A;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64804755

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499991
dbSNP (classic)	rs1060499991
ClinGen	rs1060499991
ebi	rs1060499991
HLI	rs1060499991
Exac	rs1060499991
Gnomad	rs1060499991
Varsome	rs1060499991
LitVar	rs1060499991
Map	rs1060499991
PheGenI	rs1060499991
Biobank	rs1060499991
1000 genomes	rs1060499991
hgdp	rs1060499991
ensembl	rs1060499991
geneview	rs1060499991
scholar	rs1060499991
google	rs1060499991
pharmgkb	rs1060499991
gwascentral	rs1060499991
openSNP	rs1060499991
23andMe	rs1060499991
SNPshot	rs1060499991
SNPdbe	rs1060499991
MSV3d	rs1060499991
GWAS Ctlg	rs1060499991

Max Magnitude

0

ClinVar
Risk	rs1060499991(A;A)
Alt	rs1060499991(A;A)
Reference	Rs1060499991(G;G)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64572227C>T
CLNSRC
CLNACC	RCV000474300.1,