rs1060499986

Orientation

minus

Stabilized

minus

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

Make rs1060499986(A;G)

Make rs1060499986(G;G)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64804818

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499986
dbSNP (classic)	rs1060499986
ClinGen	rs1060499986
ebi	rs1060499986
HLI	rs1060499986
Exac	rs1060499986
Gnomad	rs1060499986
Varsome	rs1060499986
LitVar	rs1060499986
Map	rs1060499986
PheGenI	rs1060499986
Biobank	rs1060499986
1000 genomes	rs1060499986
hgdp	rs1060499986
ensembl	rs1060499986
geneview	rs1060499986
scholar	rs1060499986
google	rs1060499986
pharmgkb	rs1060499986
gwascentral	rs1060499986
openSNP	rs1060499986
23andMe	rs1060499986
SNPshot	rs1060499986
SNPdbe	rs1060499986
MSV3d	rs1060499986
GWAS Ctlg	rs1060499986

Max Magnitude

0

ClinVar
Risk	rs1060499986(G;G)
Alt	rs1060499986(G;G)
Reference	Rs1060499986(A;A)
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.64572290T>C
CLNSRC
CLNACC	RCV000457794.1,