rs1060499976

Orientation

minus

Stabilized

minus

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

Make rs1060499976(G;T)

Make rs1060499976(T;T)

Reference

GRCh38.p7 38.3/150

Chromosome

11

Position

64807178

Gene

MEN1

is a	snp
is	mentioned by
dbSNP	rs1060499976
dbSNP (classic)	rs1060499976
ClinGen	rs1060499976
ebi	rs1060499976
HLI	rs1060499976
Exac	rs1060499976
Gnomad	rs1060499976
Varsome	rs1060499976
LitVar	rs1060499976
Map	rs1060499976
PheGenI	rs1060499976
Biobank	rs1060499976
1000 genomes	rs1060499976
hgdp	rs1060499976
ensembl	rs1060499976
geneview	rs1060499976
scholar	rs1060499976
google	rs1060499976
pharmgkb	rs1060499976
gwascentral	rs1060499976
openSNP	rs1060499976
23andMe	rs1060499976
SNPshot	rs1060499976
SNPdbe	rs1060499976
MSV3d	rs1060499976
GWAS Ctlg	rs1060499976

Max Magnitude

0

ClinVar
Risk	rs1060499976(C;C) rs1060499976(T;T)
Alt	rs1060499976(C;C) rs1060499976(T;T)
Reference	Rs1060499976(G;G)
Significance	Pathogenic
Disease	Multiple endocrine neoplasia Hereditary cancer-predisposing syndrome
Variation	info
Gene	MEN1
CLNDBN	Multiple endocrine neoplasia, type 1 Hereditary cancer-predisposing syndrome
Reversed	1
HGVS	NC_000011.9:g.64574650C>A; NC_000011.9:g.64574650C>G
CLNSRC
CLNACC	RCV000466988.1, RCV000491420.1,