rs1060503789

Orientation

minus

Stabilized

minus

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

Make rs1060503789(C;T)

Make rs1060503789(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64807095

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1060503789
dbSNP (classic)	rs1060503789
ClinGen	rs1060503789
ebi	rs1060503789
HLI	rs1060503789
Exac	rs1060503789
Gnomad	rs1060503789
Varsome	rs1060503789
LitVar	rs1060503789
Map	rs1060503789
PheGenI	rs1060503789
Biobank	rs1060503789
1000 genomes	rs1060503789
hgdp	rs1060503789
ensembl	rs1060503789
geneview	rs1060503789
scholar	rs1060503789
google	rs1060503789
pharmgkb	rs1060503789
gwascentral	rs1060503789
openSNP	rs1060503789
23andMe	rs1060503789
SNPshot	rs1060503789
SNPdbe	rs1060503789
MSV3d	rs1060503789
GWAS Ctlg	rs1060503789

Max Magnitude

0

ClinVar
Risk	rs1060503789(A;A) rs1060503789(T;T)
Alt	rs1060503789(A;A) rs1060503789(T;T)
Reference	Rs1060503789(C;C)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia not provided Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1 not provided Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64574567G>A; NC_000011.9:g.64574567G>T
CLNSRC
CLNACC	RCV000456598.1, RCV000484977.1, RCV000491793.1,