rs1060499987

Orientation

minus

Stabilized

minus

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

Make rs1060499987(A;A)

Make rs1060499987(A;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64809792

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499987
dbSNP (classic)	rs1060499987
ClinGen	rs1060499987
ebi	rs1060499987
HLI	rs1060499987
Exac	rs1060499987
Gnomad	rs1060499987
Varsome	rs1060499987
LitVar	rs1060499987
Map	rs1060499987
PheGenI	rs1060499987
Biobank	rs1060499987
1000 genomes	rs1060499987
hgdp	rs1060499987
ensembl	rs1060499987
geneview	rs1060499987
scholar	rs1060499987
google	rs1060499987
pharmgkb	rs1060499987
gwascentral	rs1060499987
openSNP	rs1060499987
23andMe	rs1060499987
SNPshot	rs1060499987
SNPdbe	rs1060499987
MSV3d	rs1060499987
GWAS Ctlg	rs1060499987

Max Magnitude

0

ClinVar
Risk	rs1060499987(A;A)
Alt	rs1060499987(A;A)
Reference	Rs1060499987(T;T)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1
Reversed	1
HGVS	NC_000011.9:g.64577264A>T
CLNSRC
CLNACC	RCV000472445.1,