rs1060499990

Orientation

minus

Stabilized

minus

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

Make rs1060499990(-;-)

Make rs1060499990(-;C)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64809942

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499990
dbSNP (classic)	rs1060499990
ClinGen	rs1060499990
ebi	rs1060499990
HLI	rs1060499990
Exac	rs1060499990
Gnomad	rs1060499990
Varsome	rs1060499990
LitVar	rs1060499990
Map	rs1060499990
PheGenI	rs1060499990
Biobank	rs1060499990
1000 genomes	rs1060499990
hgdp	rs1060499990
ensembl	rs1060499990
geneview	rs1060499990
scholar	rs1060499990
google	rs1060499990
pharmgkb	rs1060499990
gwascentral	rs1060499990
openSNP	rs1060499990
23andMe	rs1060499990
SNPshot	rs1060499990
SNPdbe	rs1060499990
MSV3d	rs1060499990
GWAS Ctlg	rs1060499990

Max Magnitude

0

ClinVar
Risk	rs1060499990(-;-)
Alt	rs1060499990(-;-)
Reference	Rs1060499990(C;C)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia not provided
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1 not provided
Reversed	1
HGVS	NC_000011.9:g.64577414delG
CLNSRC
CLNACC	RCV000460562.1, RCV000486690.1,