rs1060499981

Orientation

minus

Stabilized

minus

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

Make rs1060499981(A;A)

Make rs1060499981(A;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64805056

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499981
dbSNP (classic)	rs1060499981
ClinGen	rs1060499981
ebi	rs1060499981
HLI	rs1060499981
Exac	rs1060499981
Gnomad	rs1060499981
Varsome	rs1060499981
LitVar	rs1060499981
Map	rs1060499981
PheGenI	rs1060499981
Biobank	rs1060499981
1000 genomes	rs1060499981
hgdp	rs1060499981
ensembl	rs1060499981
geneview	rs1060499981
scholar	rs1060499981
google	rs1060499981
pharmgkb	rs1060499981
gwascentral	rs1060499981
openSNP	rs1060499981
23andMe	rs1060499981
SNPshot	rs1060499981
SNPdbe	rs1060499981
MSV3d	rs1060499981
GWAS Ctlg	rs1060499981

Max Magnitude

0

ClinVar
Risk	rs1060499981(A;A)
Alt	rs1060499981(A;A)
Reference	Rs1060499981(C;C)
Significance	Probable-Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MAP4K2 MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64572528G>T
CLNSRC
CLNACC	RCV000467767.1,