rs1060499974

Orientation

minus

Stabilized

minus

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

Make rs1060499974(C;T)

Make rs1060499974(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64805141

Gene	MAP4K2, MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499974
dbSNP (classic)	rs1060499974
ClinGen	rs1060499974
ebi	rs1060499974
HLI	rs1060499974
Exac	rs1060499974
Gnomad	rs1060499974
Varsome	rs1060499974
LitVar	rs1060499974
Map	rs1060499974
PheGenI	rs1060499974
Biobank	rs1060499974
1000 genomes	rs1060499974
hgdp	rs1060499974
ensembl	rs1060499974
geneview	rs1060499974
scholar	rs1060499974
google	rs1060499974
pharmgkb	rs1060499974
gwascentral	rs1060499974
openSNP	rs1060499974
23andMe	rs1060499974
SNPshot	rs1060499974
SNPdbe	rs1060499974
MSV3d	rs1060499974
GWAS Ctlg	rs1060499974

Max Magnitude

0

ClinVar
Risk	rs1060499974(T;T)
Alt	rs1060499974(T;T)
Reference	Rs1060499974(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.64572613G>A
CLNSRC
CLNACC	RCV000456454.1, RCV000486722.1, RCV000491295.1,